Brain 2011: 134; 892–902
A JOURNAL OF NEUROLOGY
The clinical and molecular genetic featuresof idiopathic infantile periodic alternatingnystagmus
Mervyn G. Thomas,1 Moira Crosier,2 Susan Lindsay,2 Anil Kumar,1 Shery Thomas,1Masasuke Araki,3 Chris J. Talbot,4 Rebecca J. McLean,1 Mylvaganam Surendran,1 Katie Taylor,5Bart P. Leroy,6 Anthony T. Moore,7,8 David G. Hunter,9 Richard W. Hertle,10,11 Patrick Tarpey,12Andrea Langmann,13 Susanne Lindner,13 Martina Brandner13 and Irene Gottlob1
1 Ophthalmology Group, School of Medicine, University of Leicester, RKCSB, PO Box 65, Leicester LE2 7LX, UK2 MRC-Wellcome Trust Human Developmental Biology Resource (Newcastle), Institute of Human Genetics, Newcastle University, International
Centre for Life, Newcastle upon Tyne NE1 3BZ, UK
3 Department of Biological Sciences, Developmental Neurobiology Laboratory, Nara Women's University, Nara 630-8506, Japan4 Department of Genetics, University of Leicester, University Road, Leicester LE1 7RH, UK5 Department of Cancer Studies and Molecular Medicine, University of Leicester, RKCSB, Leicester LE2 7LX, UK6 Department of Ophthalmology and Centre for Medical Genetics, Ghent University and Ghent University Hospital, 9000 Ghent, Belgium
7 Moorfields Eye Hospital, City Road, London EC1V 2PD, UK8 UCL Institute of Ophthalmology, London EC1V 9EL, UK9 Department of Ophthalmology, Children's Hospital Boston, Harvard Medical School, Boston, MA 02115, USA
10 Department of Ophthalmology, Children's Hospital Medical Centre of Akron, Akron, OH 44308, USA11 Northeast Ohio College of Medicine, Rootstown, OH 44272, USA12 Wellcome Trust Sanger Institute, Hinxton Cambridge CB10 1SA, UK13 Department of Ophthalmology, Medical University Graz, Auenbruggerplatz 4, 8036, Graz, Austria
Correspondence to: Prof. Irene Gottlob,Ophthalmology Group,School of Medicine,University of Leicester,RKCSB, PO Box 65,Leicester LE2 7LX,UKE-mail: firstname.lastname@example.org
Periodic alternating nystagmus consists of involuntary oscillations of the eyes with cyclical changes of nystagmus direction.
It can occur during infancy (e.g. idiopathic infantile periodic alternating nystagmus) or later in life. Acquired forms are oftenassociated with cerebellar dysfunction arising due to instability of the optokinetic-vestibular systems. Idiopathic infantile peri-odic alternating nystagmus can be familial or occur in isolation; however, very little is known about the clinical characteristics,genetic aetiology and neural substrates involved. Five loci (NYS1-5) have been identified for idiopathic infantile nystagmus;three are autosomal (NYS2, NYS3 and NYS4) and two are X-chromosomal (NYS1 and NYS5). We previously identified theFRMD7 gene on chromosome Xq26 (NYS1 locus); mutations of FRMD7 are causative of idiopathic infantile nystagmus influen-cing neuronal outgrowth and development. It is unclear whether the periodic alternating nystagmus phenotype is linked toNYS1, NYS5 (Xp11.4-p11.3) or a separate locus. From a cohort of 31 X-linked families and 14 singletons (70 patients) withidiopathic infantile nystagmus we identified 10 families and one singleton (21 patients) with periodic alternating nystagmus ofwhich we describe clinical phenotype, genetic aetiology and neural substrates involved. Periodic alternating nystagmus was not
Received September 3, 2010. Revised November 8, 2010. Accepted November 9, 2010. Advance Access publication February 8, 2011ß The Author (2011). Published by Oxford University Press on behalf of the Guarantors of Brain. All rights reserved.
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Idiopathic infantile PAN
Brain 2011: 134; 892–902
detected clinically but only on eye movement recordings. The cycle duration varied from 90 to 280 s. Optokinetic reflex was notdetectable horizontally. Mutations of the FRMD7 gene were found in all 10 families and the singleton (including three novelmutations). Periodic alternating nystagmus was predominantly associated with missense mutations within the FERM domain.
There was significant sibship clustering of the phenotype although in some families not all affected members had periodicalternating nystagmus. In situ hybridization studies during mid-late human embryonic stages in normal tissue showed restrictedFRMD7 expression in neuronal tissue with strong hybridization signals within the afferent arms of the vestibulo-ocular reflexconsisting of the otic vesicle, cranial nerve VIII and vestibular ganglia. Similarly within the afferent arm of the optokinetic reflexwe showed expression in the developing neural retina and ventricular zone of the optic stalk. Strong FRMD7 expression wasseen in rhombomeres 1 to 4, which give rise to the cerebellum and the common integrator site for both these reflexes (vestibularnuclei). Based on the expression and phenotypic data, we hypothesize that periodic alternating nystagmus arises from instabilityof the optokinetic-vestibular systems. This study shows for the first time that mutations in FRMD7 can cause idiopathic infantileperiodic alternating nystagmus and may affect neuronal circuits that have been implicated in acquired forms.
Keywords: periodic alternating nystagmus; FRMD7; optokinetic reflex; vestibulo-ocular reflex; in situ hybridizationAbbreviation: PAN = periodic alternating nystagmus
form of PAN often responds well to specific drugs such as baclo-
fen (Halmagyi et al., 1980).
Nystagmus is defined as the involuntary rhythmic oscillations of
Idiopathic infantile nystagmus is a genetically heterogeneous
the eyes, with a reported prevalence of approximately 2.4 in 1000
condition with X-linked, autosomal dominant and autosomal re-
(Sarvananthan et al., 2009). There is significant negative social
cessive modes of inheritance reported. To date, five chromosomal
stigma and relatively poor visual function scores reported with
loci (NYS 1–5) have been described in the literature associated
this condition (Pilling et al., 2005). In infantile nystagmus, these
with idiopathic infantile nystagmus (Table 1). Within the NYS1
oscillations are horizontal and conjugate and are characterized by
locus (Xq26.2), the FRMD7 gene was identified, mutations of
two components: (i) a slow drift of the eyes (called the slow
which cause X-linked idiopathic infantile nystagmus (Tarpey
phase); followed by (ii) a corrective fast eye movement (called
et al., 2006; Schorderet et al., 2007; Zhang et al., 2007).
the quick phase) that is responsible for realigning the fovea to
Previous studies have shown that the penetrance among female
the object of interest. In idiopathic infantile periodic alternating
carriers is 50% (Tarpey et al., 2006; Thomas et al., 2008).
nystagmus (PAN), the direction of the quick phase and slow
Expression of FRMD7 has been shown in neuronal tissue in the
phase alternates periodically with time. This phenotype of nystag-
developing retina, mid and hind brain (Tarpey et al., 2006;
mus is distinct from other nystagmus forms due to the periodic
Betts-Henderson et al., 2009), although it is not clear which spe-
time component. Acquired forms of PAN are also reported and
cific gaze control systems are affected by mutations in the gene.
arise due to instability of the vestibulo-optokinetic systems (Leigh
Unaffected female carriers can have a subnormal optokinetic nys-
et al., 1981). Animal and mathematical models for acquired PAN
tagmus gain (Thomas et al., 2008). Recent studies in neuro-2A
have demonstrated how instability of the velocity storage mech-
cells have demonstrated a role for FRMD7 in neuronal outgrowth
anism for vestibular eye movements and an adaptive mechanism
and development (Betts-Henderson et al., 2009).
for this instability can result in a periodicity of oscillations of 4 min
Idiopathic infantile PAN is considered to be a subtype of idio-
(Waespe et al., 1985; Leigh and Khanna, 2006). It has also been
pathic infantile nystagmus; however, its diagnosis has different
shown that patients with acquired PAN have abnormalities of
optokinetic nystagmus, with some patients having no optokinetic
(Reinecke, 1997). The first report of familial idiopathic infantile
nystagmus response and the PAN cycle continues through the
PAN was by Huygen and colleagues (1995), where both mother
optokinetic nystagmus stimuli (Baloh et al., 1976). The acquired
Table 1 The nystagmus loci
(Tarpey et al., 2006)
(Kerrison et al., 1996)
(Klein et al., 1998)
(Ragge et al., 2003)
NYS 5 (Xp11.4-p11.3)
(Cabot et al., 1999)
= Online Mendelian Inheritance in Man.
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M. G. Thomas et al.
Shallo-Hoffmann et al. (1999, 2004) reported a case of idiopathic
consisted of square-wave contrast gratings of 2.2 cycle size and
infantile PAN with an X-linked history of nystagmus. Hertle et al.
Michelson contrast 0.88 cd/m2. Optokinetic nystagmus was tested at
(2005) described another family spanning three generations, with
20/s velocity in both horizontal (stimulus direction: rightwards and
a phenotype of PAN in all four patients examined with eye move-
leftwards) and vertical directions (upwards and downwards). For fur-ther details of the experimental setup see Thomas et al. (2008).
ment recordings. Based on an X-linked mode of inheritance and
Informed consent was obtained from all subjects participating in this
the distinct phenotype consistently seen in all generations it was
study. The study adhered to the tenets of the Declaration of Helsinki
assumed that a unique locus for idiopathic infantile PAN was
and was approved by the local Ethics Committee.
present on the X-chromosome. However, no molecular geneticstudies were performed in these families to substantiate that aseparate locus is present for idiopathic infantile PAN. There is
Sequencing and mutation analysis
some evidence for an additional locus for idiopathic infantile nys-
Bidirectional sequence analysis of the exons and intron/exon junctions
tagmus on the X-chromosome. Cabot et al. (1999) reported a four
of the FRMD7 gene were performed using DNA from the proband
generation French family with X-linked idiopathic infantile nystag-
within each of the new families and singletons with idiopathic infantile
mus. Linkage analysis showed mapping to Xp11.4-11.3 between
nystagmus where no genetic test for FRMD7 had been performed
the polymorphic markers DXS8015 and DXS1003, however, these
previously. Primer details, expected product sizes and annealing tem-
investigators did not describe the type of nystagmus in this family.
perature are shown in Table 2. Mutation analysis software Seqscape
Due to the limited phenotypic data in the literature it is currently
version 2.1.1 (Applied Biosystems) was used for base calling and align-
unknown whether idiopathic infantile PAN occurs in nystagmus
ment of the contigs. The Genbank file (NM_194277.2) was imported
with other inheritance patterns. In the family described by
into Seqscape and used as the reference complementary DNA se-
Huygen and colleagues (1995), the inheritance pattern is not
quence for contig alignment. Base position + 1 corresponded to A ofthe translation initiation codon ATG. Intronic sequence changes were
clear. In this study we present evidence showing that mutations
identified based on the FRMD7 genomic sequence (NC_000023.10)
of the FRMD7 gene can be associated with PAN. We report three
and amino acid changes were identified based on the reference protein
novel mutations and eight previously described mutations of the
sequence (NP_919253.1). Allelic variations were assessed against the
FRMD7 gene associated with PAN. Furthermore, we highlight the
sequence data from 300 male controls (without nystagmus).
spectrum of variable phenotypes associated with FRMD7 muta-tions and present evidence that expression of FRMD7 correlates to
neuronal circuits that have also been associated with acquired
In situ hybridization experiments
Human embryonic and foetal tissues were obtained from theMRC-Wellcome
Trust Human Developmental
(www.hdbr.org; Lindsay and Copp, 2005), Institute of Human
Materials and methods
Genetics, Newcastle University. The samples were collected with ap-propriate maternal consents and ethical approval by the Newcastle and
Patients and clinical examinations
North Tyneside Research Ethics Committee. Tissue sections used em-bryos with a normal karyotype and morphology. Tissue sections from
Using eye movement recordings we examined a cohort of 31 families
eight samples were analysed from Carnegie Stage 16 (37 days post-
with X-linked idiopathic infantile nystagmus and 14 singletons (total of
conception; n = 1); Carnegie Stage 19 (47 days post-conception;
70 patients). Fifteen of the families were previously described to have
n = 3); Carnegie Stage 22 (54 days post-conception; n = 2) and
FRMD7 mutations (Tarpey et al., 2006) and four families did not have
Carnegie Stage 23 (56 days post-conception; n = 2). The stage of
FRMD7 mutations. For the remaining 12 families with idiopathic
embryonic development was determined by assessment of external
infantile nystagmus, the genotype was not yet determined. Among
morphology as described in Bullen and Wilson (1997) and O'Rahilly
the singletons, we included the previously identified three singletons
and Muller (1987).
with FRMD7 mutations (Tarpey et al., 2006) and 11 singletons with
In situ hybridizations were preformed as previously described
idiopathic infantile nystagmus that were not yet sequenced. Within
(Moorman et al., 2001) with some modifications. Briefly, sections
this cohort we identified 10 families (Fig. 1) and one singleton with
were dewaxed in xylene, gradually hydrated in decreasing ethanol
idiopathic infantile PAN (total of 21 patients). In our study population,
concentrations before incubation in proteinase K (20 mg/ml) at room
idiopathic infantile PAN occurred in 18 males and in three females.
temperature, followed by fixation using 4% paraformaldehyde in
Detailed ophthalmic examination was performed in all patients. At
phosphate buffered saline. Background was reduced by treating with
least one affected patient within each family underwent electrodiag-
0.1 M triethanolamine pH 8. Sections were air dried and the sense or
nostic examinations according to the International Society for Clinical
antisense probes [300 ng labelled probe per 100 ml of DIG Easy Hyb
Electrophysiology of Vision standards (visually evoked potentials and
mix (Roche)] were added for hybridization at 68C overnight. Next
electroretinography) to exclude other infantile forms of nystagmus
day sections were washed in 5 followed by 2 saline sodium citrate
such as those associated with albinism or retinal diseases. Eye move-
buffer at 60C then incubated with anti-digoxigenin alkaline phosphat-
ment recordings were performed (EyeLink II, 500 Hz, SR Research,
ase Fab fragments (Roche) diluted 1:1000 at 4C overnight. Sections
Toronto, Canada) using a central fixation task over a prolonged
were then washed and expression detected using NBT/BCIP (20 ml/ml;
period of 5 min to detect idiopathic infantile PAN. Several members
Roche) in 0.1 M Tris (pH 9.5)/0.1 M NaCl (Buffer 2) in the dark at
of most families and all the singletons underwent the prolonged fix-
room temperature. Developing was stopped by rinsing slides in Buffer
ation task (Fig. 1).
2 then distilled water. Sections were mounted using Aquamount and
In addition, optokinetic nystagmus was tested in all affected patients
analysed using a Zeiss Axioplan 2 microscope. Images were captured
with idiopathic infantile PAN. The optokinetic nystagmus stimulus
with Zeiss Axiovision 4 imaging system.
Idiopathic infantile PAN
Brain 2011: 134; 892–902
Figure 1 Families with idiopathic infantile PAN. In Families 1–4 eye movement recordings were performed in three or more affectedindividuals, whereas in Families 4–7 eye movement recordings were obtained in two or more affected individuals. In Families 8–10 eyemovement recordings were only performed in one affected individual.
0.2 LogMAR. Three patients with idiopathic infantile PAN had aslight anomalous head posture between 5–10. However, in onlyone patient was the head posture noticed to alternate to the right
Clinical characteristics and eye
or left on two different examination days. None of the patients
with idiopathic infantile PAN had strabismus. All had some degreeof stereopsis; the range of stereoacuity was 85–55000 with a
The pedigrees of patients diagnosed with idiopathic infantile PAN
median stereoacuity of 15000.
are shown in Fig. 1. Among the 10 families, we were able to
Idiopathic infantile PAN was not diagnosed clinically in any of
perform eye movement recordings in 26 affected patients, of
the families or the singletons. However, the use of eye movement
whom 20 had idiopathic infantile PAN (Fig. 1). The phenotypes
recordings during a prolonged duration of fixation (5 min) aided
in affected members of Family 2 have previously been described
the diagnosis of idiopathic infantile PAN. An example of original
by Hertle et al. (2005).
eye movement recordings from Family F3 is shown in Fig. 2. In
The best-corrected visual acuity in our cohort of patients with
Families F1, F3, F4 and F7 we observed phenotypic heterogeneity
PAN ranged from 0.0 LogMAR to 0.54 LogMAR with a median of
as not all the examined patients had idiopathic infantile
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M. G. Thomas et al.
Table 2 Forward and reverse primer sequences, product
families; similarly within the 11 singletons we identified mutations
sizes and melting temperature (Tm) used to amplify
in two out of 11 singletons. Thus, the total cohort consisted of a
total of 24 families and five singletons with an FRMD7 mutation;the remaining seven families and nine singletons had no such mu-
tations. In all 10 of the idiopathic infantile PAN families and the
singletons with idiopathic infantile PAN, there were mutations ofthe FRMD7 gene, three of which were novel. A summary of the
mutations and domains affected are shown in Fig. 4.
The three novel mutations were in Family F8, F9 and singleton
S1. Family F8 had a missense mutation (c.47T 4 C) in exon 1,
resulting in the substitution of phenylalanine by serine at position
16 (p.F16S). Sequence analysis of the proband in family F9 re-
vealed a splice-site mutation (c.58-1G 4 A) at the 30-end of
intron 1. This results in the loss of the conserved splice acceptor
residue. The effects of the mutation were predicted using the al-
ternative splice-site predictor (Wang and Marı´n, 2006), and con-
sidered pathological due to exon skipping resulting in a messenger
RNA transcript with exon 2 missing. The singleton S1, had a mis-
sense mutation (c.811T 4 A) in exon 9 resulting in a substitution
of cysteine to serine at position 271 (p.C271S). Both missense
mutations at amino acid positions 16 and 271 were considered
pathological as they involved residues that were identical within
invariant blocks in the species Mus, Gallus, Xenopus and
Tetraodon. Furthermore, the structural effects of these mutations
were elucidated based on the known crystal structure of the clo-
sest orthologue (PDB Accession ID: 1GG3) and secondary struc-
ture prediction of the FRMD7 protein sequence using Emboss
Garnier (Garnier et al., 1978). Finally the stability of the mutant
protein was assessed using I-Mutant (v2.0) (Capriotti et al., 2005)
and Coot (v0.6) (Emsley and Cowtan, 2004). The amino acid
change C271S would disrupt a large alpha-helical domain in the
wild-type structure. Similarly, the amino acid change F16S is likely
to disrupt adjacent secondary structure. Consequently, both mis-sense mutations, F16S and C271S, decrease the stability of themutant protein (due to a decrease in the free energy value).
Six of the eight remaining families (F1, 2, 3, 4, 7 and 10) all
PAN (Fig. 2). Among the families with idiopathic infantile PAN, six
revealed missense mutations of the FRMD7 gene. These mutations
of 26 subjects in which eye movements were performed did not
have been reported previously and their translational effects have
have PAN. Overall, the time period for the idiopathic infantile PAN
been described (Tarpey et al., 2006). Family F5 and F6 were the
cycle varied between 90 and 260 s and the singleton had a peri-
only families that had a nonsense mutation (c. 1003C 4 T) result-
odicity of 280 s. All family (F1–F10) members with idiopathic in-
ing in a premature stop codon at amino acid position 335 (p.
fantile PAN had a jerk-related or dual jerk nystagmus. In family
R335X). Family F2 was previously reported with an idiopathic in-
members without idiopathic infantile PAN (F1, III:3; F3, II:2 and 4;
fantile PAN phenotype and an X-linked inheritance (Hertle et al.,
F4, III:1 and 2; F7, II:1;) the predominant nystagmus waveform
2005). Sequence analysis of this family revealed a missense mu-
tation (c.70G 4 A) resulting in hemizygous replacement of glycine
None of the patients with idiopathic infantile PAN showed an
with arginine at position 24 (p. G24R). The amino acid changes as
optokinetic response for either horizontal stimulus directions
a result of the missense mutations in families F1 (L231V), F2
(rightwards and leftwards). The PAN cycle continued through
(G24R), F3 (C271Y), F4 (A266P), F7 (A226T) and F10 (S340L)
the optokinetic nystagmus testing and was not changed by the
are associated with a decrease in the free energy value that is
optokinetic nystagmus stimuli (Fig. 3). Vertical optokinetic nystag-
likely to destabilize the mutant protein.
mus was seen in all patients in both directions (upwards anddownwards).
Expression of FRMD7
In situ hybridization experiments showed strong hybridization sig-nals from the structures involved in setting up the vestibulo-ocular
Among the 12 families with idiopathic infantile nystagmus we
reflex and optokinetic reflex arc, this included the developing
identified mutations in nine out of 12 previously uncharacterized
Idiopathic infantile PAN
Brain 2011: 134; 892–902
Figure 2 Original eye movement recordings from Family F1. Overviews of the three phases of the PAN cycle and excerpts from withineach phase of the cycle are shown in this figure. A typical PAN cycle consists of three phases: (i) left jerk (LJ), where the quick phase isdirected to the left; (ii) a quiet phase (QP), where the intensity of the nystagmus is minimal; and (iii) a right jerk (RJ), where the quick phaseis directed to the right. One of the examined family members (III:3) did not have PAN, but a pendular (P) nystagmus. Scale for the excerptsare shown in the bottom right with waveform deflection upwards and downwards representing horizontal eye movements to the right andleft, respectively.
retina (Fig. 5A–E). Expression is detected in the ventricular zone of
recordings and most patients had relatively good visual acuity
the neural retina and optic stalk (Fig. 5B). In structures of the
(median: 0.2 LogMAR) and stereoacuity (median: 15000). Fewer
vestibulo-ocular reflex, FRMD7 is expressed in the otic vesicle and
females were affected since FRMD7-related infantile nystagmus
vestibulocochlear ganglion (Fig. 5C). The vestibular nuclei, which
represents a disorder associated with variable penetrance in fe-
arise partly from the ventricular zone of rhombomeres 2, 3 and 4,
males (Tarpey et al., 2006; Thomas et al., 2008). The PAN cycle
form the horizontal neural integrator, which is an important structure
length varied from 90–280 s and none of the patients with idio-
in the vestibulo-ocular reflex and optokinetic reflex arcs. FRMD7
pathic infantile PAN had a horizontal optokinetic reflex. We show
expression is seen in the ventricular zone of rhombomeres 2, 3 and
that FRMD7 is expressed within developing vestibulo-ocular reflex
4 (Fig. 5D) as well as in the developing cerebellum (Fig. 5E). The
and optokinetic reflex arcs, which identifies the likely neural sub-
cerebellum arises entirely from rhombomere 1 and its ventricular
strates involved in idiopathic infantile PAN and in FRMD7-related
zone gives rise to neuroblasts that migrate on radial glia to develop
infantile nystagmus. We identified 11 mutations in 10 families and
into the cerebellar nuclei and Purkinje cells in the cerebellar cortex.
one singleton and describe both the phenotypic and translational
FRMD7 is expressed in differentiating and migrating neurons as well
effects of these mutations. In our cohort of families, the predom-
as in the ventricular zone, for example in the cerebellum and rhom-
inant class of mutation associated with this phenotype were mis-
bomeres 3 and 4 in the hindbrain (Fig. 5D and E) but also in the
sense mutations (8/11) though both truncating (2/11) and
subpallium in the forebrain (data not shown).
splice-site (1/11) mutations are also seen. Ten of the 11 mutationsresulted in amino acid changes within functionally significant do-
mains (FERM-N, FERM-C and FA).
From a clinical point of view PAN is typically under-diagnosed
In this study we show for the first time that idiopathic infantile
(Abadi and Pascal, 1994; Gradstein et al., 1997; Abadi and Bjerre,
PAN can be associated with mutations of the FRMD7 gene.
2002) as it can often only be identified on eye movement record-
Idiopathic infantile PAN was only detected using eye movement
ings during an extended fixation task to demonstrate the
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M. G. Thomas et al.
Figure 3 Compressed eye movement recordings showing an overview of the various phases of the PAN cycle (A). In the above exampleone cycle consists of right jerk (RJ) followed by a quiet phase (QP), left jerk phase (LJ) and another quiet phase (QP). Upward deflection ofthe horizontal (H) position and velocity trace represents right-beating nystagmus and downward deflection represents left-beating nys-tagmus. The optokinetic response was measured for optokinetic nystagmus stimuli (B) moving in the horizontal [rightwards (L!R) andleftwards (R!L)] and in the vertical direction [downwards (U!D) and upwards (D!U)]. The patient (II-PAN) shows no horizontaloptokinetic response to the stimulus; the nystagmus is unchanged in the right jerk phase during optokinetic nystagmus testing. Howeverfor the vertical optokinetic nystagmus stimuli, a vertical optokinetic response is seen in the vertical trace (V) for the patient. The idiopathicinfantile PAN cycle was not changed by the horizontal optokinetic nystagmus stimuli as shown in (C). The transition (QP) between left jerkand right jerk is seen during an extended horizontal optokinetic nystagmus task.
periodicity of the nystagmus and its three phases. A recent study
nystagmus patients have PAN. Interestingly, in the idiopathic in-
estimated that 15% of all infantile nystagmus syndrome patients
fantile PAN incidence study by Shallo-Hoffmann and colleagues
have PAN (Hertle et al., 2009). In contrast, Shallo-Hoffmann et al.
(1999, 2004), a family with X-linked PAN was described though
(1999) showed that a higher proportion of 39% of congenital
no genetic diagnosis was provided. We noticed the occurrence of
Idiopathic infantile PAN
Brain 2011: 134; 892–902
Figure 4 Country of origin, mutations of the FRMD7 gene in the families (F1–10) and singleton (S1) with idiopathic infantile PAN areshown in (A). The electropherograms from the respective families and singleton are shown with the wild-type allele (WA) represented ontop of the mutant allele (MA). All mutant electropherograms show hemizygous mutations of the FRMD7 gene except for the femaleprobands in Families F4 and F10, where a heterozygous mutation is shown. The type of mutation and domain affected is shown in (B).
Missense mutations were the most common and changes to amino acid at positions 271 and 335 occurred in two families (271: F3 and S1;335: F5 and F6). F1 = Family 1; S1 = Singleton 1; B41 = Band 4.1; FA = FERM adjacent domain.
Brain 2011: 134; 892–902
M. G. Thomas et al.
Figure 5 FRMD7 expression in developing human brain. Panel A shows low magnification views of the sections from whichhigher magnification views are shown in (B–E). (F) gives a simplified overview of the vestibulo-ocular reflex (VOR) and optokinetic reflex(OKR) arcs indicating the afferent arm of the reflex arc starting at the semicircular canals (SCC) and retina followed by the cranial nerves(CN) involved in the respective arcs. The neural signal is integrated at the vestibular nucleus (VN) that is subject to the feedback loopthrough the cerebellum. The efferent arm of the reflex consists of the oculomotor nerves innervating the effector organ i.e. the extraocularmuscles (EOM). (A) shows the following images from left to right: Carnegie Stage 16 section through forebrain and hindbrain; CarnegieStage 19 whole embryo sagittal section; Carnegie Stage 22 section through midbrain and hind brain; Carnegie Stage 23 section throughmidbrain, hindbrain and forebrain; and Carnegie Stage 23 head sagittal section. In (C–F) images of sections hybridized with antisenseprobes (signal detected as purple stain) are shown above corresponding sections hybridized to sense control probes (no signal detected).
Scale bar for the low magnification images (A) represents 1 mm for all images except the Carnegie Stage 16 image where the scalebar is 0.5 mm. For all high magnification images (B–E) the scale bar represents 0.3 mm except the preoptic image (Carnegie Stage 23)where it represents 0.6 mm. nr = neural retina; os = optic stalk; po = preoptic area; ov = otic vesicle; vc = vestibulocochlear ganglion;Rh1–4 = rhombomere 1–4.
idiopathic infantile PAN, using eye movement recordings, in at
infantile nystagmus whereas 82% were associated with albinism.
least one family member with an FRMD7 mutation in 10/31
The incidence of PAN with both albinism and FRMD7 mutations
(32%) families and 1/14 (7%) singletons. This suggests that
suggests that there may be a common mechanism in the occur-
most patients with idiopathic infantile PAN are likely to have a
rence of PAN in these two disorders.
family history of nystagmus and it is important to screen for
The FRMD7 protein is homologous to the FARP1 and FARP2
FRMD7 mutations. Diagnosing PAN is important since it has dif-
proteins; particularly at the N-terminus. Previous studies have
ferent therapeutic implications compared with other forms of in-
shown that FARP1 and FARP2 are involved in neurite outgrowth
fantile nystagmus. The Kestenbaum procedure is used in idiopathic
and branching (Toyofuku et al., 2005; Zhuang et al., 2009).
infantile nystagmus to correct anomalous head posture if it is con-
Recently it has been demonstrated that knockdown of FRMD7
stantly directed towards one side. However it is inappropriate in
in neuro-2A cells results in shorter neurites, suggesting a role
patients with PAN since it does not correct anomalous head pos-
in axonogenesis or dendritogenesis (Betts-Henderson, et al.,
ture which can alternate to both sides as in idiopathic infantile
2009). We found expression of FRMD7 within the developing
PAN or may even accentuate the head position to one side
vestibulo-ocular reflex and optokinetic reflex arcs. In this study
(Gradstein et al., 1997). Abadi and Bjerre (2002) showed that
we observed that all patients with PAN and FRMD7 mutations
among the cohort of patients with PAN, 18% were idiopathic
had no optokinetic nystagmus response. Previous phenotypic
Idiopathic infantile PAN
Brain 2011: 134; 892–902
studies in FRMD7-related infantile nystagmus have shown that the
1981; Furman et al., 1990). In this study we observed that the
optokinetic nystagmus gain is lower or no optokinetic nystagmus
time period for idiopathic infantile PAN varies from 90–280 s. Only
response is detected in affected individuals with FRMD7 mutations
one of our patients had a time period of 90 s, whereas the re-
(Self et al., 2007). There are also reports of reversal of optokinetic
maining had a time period 4190 s. Thus, there is some similarity
nystagmus in patients with congenital nystagmus (Halmagyi et al.,
in the periodicity of the idiopathic infantile PAN cycle when com-
1980), albino rabbits (Collewijn et al., 1978) and achiasmatic fish
pared with the acquired PAN. The neuronal substrates implicated
(Huang et al., 2006), findings suggested by the authors to result
in acquired PAN and phenotypic data from patients with acquired
from miswiring within the optokinetic nystagmus arcs. In unaffect-
PAN are closely related to the phenotypic and expression results
ed carriers of FRMD7 mutation a subnormal optokinetic nystag-
highlighted in this study. This also suggests some similarity in the
mus gain has been reported (Thomas et al., 2008). This suggests
aetiological mechanisms between infantile and acquired PAN.
that the optokinetic system is involved in this disorder and we
Acquired forms of PAN have been treated successfully using
have now provided substantial evidence from the expression stu-
baclofen (a GABA agonist). Baclofen suppresses the velocity-
dies that FRMD7 is expressed within the neural substrates in the
storage mechanism possibly by reinforcing the action of the
developing optokinetic nystagmus and vestibulo-ocular reflex arcs.
inhibitory GABAergic Purkinje cells from the nodulus to the
However the expression is not restricted to these tissues (e.g. ex-
vestibular nuclei. Some congenital forms respond occasionally to
pression is also detected in the midbrain, Fig. 5A). This provides
baclofen (Solomon et al., 2002; Comer et al., 2006). It would
general evidence of the neuronal networks involved in FRMD7-
therefore be interesting to see whether this subset of a phenotyp-
related infantile nystagmus. Based on the in vitro assays in
ically homogenous population has a different therapeutic response
FRMD7 and studies from homologous proteins (FARP1 and
compared with the other phenotypes encountered with both
FARP2) there may be miswiring of the developing optokinetic
FRMD7 patients and non-FRMD7 patients (Thomas et al., 2008).
nystagmus and vestibulo-ocular reflex systems, thus predisposing
In conclusion, we have shown that mutations in the FRMD7
to the phenotypes of PAN and FRMD7-related infantile nystag-
gene form the genetic basis of idiopathic infantile PAN.
mus. Phenotypic data (not confined to PAN) from patients with
Expression and phenotypic data suggest that congenital PAN
albinism also suggest that vestibulo-ocular reflex and optokinetic
arises from instability of the optokinetic-vestibular systems.
nystagmus systems are affected (Yee et al., 1980; Demer and Zee,1984). The higher prevalence of PAN in patients with albinism (as
suggested by Abadi and Bjerre in 2002) may be due to the mis-routing of the retinogeniculate fibres, which may predispose to
The URLs for data presented herein are as follows:
instability within the optokinetic reflex arc. Therefore the PANphenotype may represent a part of the spectrum of infantile nys-
Online Mendelian Inheritance in Man (OMIM), http://www.ncbi
tagmus forms depending on the degree of instability of the
vestibulo-optokinetic systems. However, the presence of sibship
clustering (seen in the larger families F1, F2 and F3) and familial
involvement of the PAN phenotype may suggest that certain mu-
tations of the FRMD7 gene predispose to the PAN phenotype. For
example the R335X mutation was seen in two families of different
Multiple sequence alignment program for DNA or proteins
descent, similarly mutations at amino acid position 271 (F3: C271Y
and singleton C271S) in one family and the singleton resulted
The European Molecular Biology Open Software Suite (EMBOSS),
both in idiopathic infantile PAN phenotype. The differences in
phenotype between patients could possibly be due to variable
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Moir R, Stones-Havas S, Thierer T, Wilson A (2010) Geneious
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The aetiology of acquired PAN has been associated with dys-
function of the cerebellum, including cerebellar degenerations,
We would like to thank the subjects for their participation in this
cerebellar tumours, multiple sclerosis and other mass lesions invol-
study. The human embryonic and foetal material was provided
ving the cerebellum (Leigh et al., 1981; Furman et al., 1990;
by the Joint MRC-Wellcome Trust Human Developmental
Matsumoto, et al., 2001; Hashimoto et al., 2003). Leigh and col-
Biology Resource (http://www.hdbr.org) at the IHG, Newcastle-
leagues (1981) hypothesized that acquired PAN arises as a result
upon-Tyne, UK. We also acknowledge the NIHR (Moorfields Eye
of instability within the optokinetic-vestibular system. Phenotypic
hospital BMRC) for the support.
data from patients with acquired PAN also suggest that thepatients had no optokinetic function and the optokinetic nystag-mus stimuli did not perturb the PAN cycle (Baloh et al., 1976;
Leigh et al., 1981). The time period for one PAN cycle in acquiredforms varies from 200–240 s (Baloh et al., 1976; Leigh et al.,
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UNIVERSIDAD FRANCISCO DE PAULA SANTANDER OCAÑA Documento Revisión FORMATO HOJA DE RESUMEN 10-04-2012 PARA TRABAJO DE GRADO Dependencia Aprobado DIVISIÓN DE BIBLIOTECA SUBDIRECTOR ACADEMICO RESUMEN - TESIS DE GRADO XIOMARA PATRICIA TRUJILLO RINCON
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