Tremor and Other Hyperkinetic Movements

Case Reports

TBC1D24 Mutations in a Sibship with Multifocal Polymyoclonus

Adeline Ngoh1,2†, Jose Bras3,4†, Rita Guerreiro3,4†, Amy McTague1,2, Joanne Ng1,2, Esther Meyer1, W. Kling Chong5, Stewart Boyd6, Linda MacLellan7, Martin Kirkpatrick8 & Manju A. Kurian1,2*

1Neurosciences Unit, University College London, Institute of Child Health, London, UK, 2Department of Neurology, Great Ormond Street Hospital for Children NHS Foundation Trust, London, UK, 3Department of Molecular Neuroscience, UCL Institute of Neurology, London, UK, 4Department of Medical Sciences and Institute of Biomedicine – iBiMED, University of Aveiro, Aveiro, Portugal, 5Department of Neuroradiology, Great Ormond Street Hospital for Children NHS Foundation Trust, London, UK, 6Department of Neurophysiology, Great Ormond Street Hospital for Children NHS Foundation Trust, London, UK, 7NHS Highland, UK, 8Tayside Children’s Hospital, Dundee, UK

Abstract

Background: Advances in molecular genetic technologies have improved our understanding of genetic causes of rare neurological disorders with features of myoclonus.

Case Report: A family with two affected siblings, presenting with multifocal polymyoclonus and neurodevelopmental delay, was recruited for whole-exome sequencing following unyielding diagnostic neurometabolic investigations. Compound heterozygous mutations in TBC1D24, a gene previously associated with various epilepsy phenotypes and hearing loss, were identified in both siblings. The mutations included a missense change c.457G>A (p.Glu157Lys), and a novel frameshift mutation c.545del (p.Thr182Serfs*6).

Discussion: We propose that TBC1D24-related diseases should be in the differential diagnosis for children with polymyoclonus.

Keywords: TBC1D24, myoclonus

Citation: Ngoh A, Bras J, Guerreiro R, et al. TBC1D24 mutations in a sibship with multifocal polymyoclonus. Tremor Other Hyperkinet Mov. 2017; 7. doi: 10.7916/D8Q52VBV

*To whom correspondence should be addressed. E-mail: manju.kurian@ucl.ac.uk

These authors contributed equally to the manuscript.

Editor: Elan D. Louis, Yale University, USA

Received: January 25, 2017 Accepted: March 16, 2017 Published: April 13, 2017

Copyright: © 2017 Ngoh et al. This is an open-access article distributed under the terms of the Creative Commons Attribution–Noncommercial–No Derivatives License, which permits the user to copy, distribute, and transmit the work provided that the original authors and source are credited; that no commercial use is made of the work; and that the work is not altered or transformed.

Funding: A.N. is funded by a Guarantors of Brain Entry Fellowship and an Action Medical Research Training Fellowship. J.B. and R.G.’s work is supported by Fellowships from the Alzheimer’s Society. A.M. and J.N. are funded by Medical Research Council Clinical Research Training Fellowships. A.M. also receives funding from Medical Research Foundation, Child Brain Research and Young Epilepsy; and J.N. is also supported by Great Ormond Street Hospital Children’s Charities. M.A.K. is funded by a Wellcome Trust Intermediate Clinical Fellowship and receives funding from the Rosetrees Trust, Gracious Heart Charity Foundation Great Ormond Street Hospital Children’s Charities (GOSHCC) Child Brain Research and Rachel Marie Trafford Trust.

Financial Disclosures: None.

Conflict of Interest: The authors report no conflict of interest.

Ethics Statement: All patients that appear on video have provided written informed consent; authorization for the videotaping and for publication of the videotape was provided.

Introduction

Myoclonus is defined as a sudden, brief (less than 100 ms), shock-like muscle contraction involving agonist and antagonist muscles, leading to a sudden jerky movement.1 The lifetime prevalence of myoclonus is estimated to be 8.6 cases per 100,000 population.2 Physiological myoclonus, in the form of hiccoughs or hypnic jerks, is easily recognized. Pathological myoclonus has a wide range of etiologies including acquired/hypoxic neurological injury, as well as neoplastic, infectious, post-infectious, metabolic, and genetic causes. There are a number of ways in which myoclonus is classified, including by anatomical/physiological origin (cortical, subcortical, spinal, peripheral), or by etiology. In the approach to pathological myoclonus, it is useful to consider the distribution of myoclonus, age of onset, insidious/acute onset, triggering/alleviating factors and associated signs or symptoms (Supplementary Table 1).

Recently, advances in molecular genetic technologies have enabled accelerated gene discovery, adding to our understanding of rare neurological disorders, including myoclonus (Supplementary Table 1).

We describe two siblings with infantile-onset multifocal polymyoclonus at rest who were found on whole-exome sequencing to have mutations in TBC1D24, a gene previously associated with various epilepsy phenotypes (including familial infantile myoclonic epilepsy, migrating partial seizures of infancy),313 hearing impairment,1417 and DOORS (deafness, onychodystrophy, osteodystrophy, mental retardation, and seizures) syndrome.18 Prolonged electroencephalograms (EEGs) revealed no epileptiform features; furthermore, multiple EEGs captured episodes of polymyoclonus and demonstrated no EEG correlation.

To our knowledge, this is the first report of TBC1D24 mutations in a phenotype with prolonged, multifocal polymyoclonus as the main presenting feature with no discernible features of epilepsy.

Case report

A family with two affected children was ascertained and recruited for molecular genetic analysis. The participating family gave written informed consent and the study was performed in accordance with the Declaration of Helsinki. Genomic DNA from the affected individuals, and both parents was extracted from peripheral lymphocytes by standard techniques.

Whole-exome sequencing was carried out in both affected individuals using Illumina’s TruSeq Exome Enrichment kit (Illumina, Inc San Diego, California, USA), according to manufacturer’s recommendations. Sequencing was performed on Illumina HiSeq2000 using 100-bp paired-end reads. Data were analyzed following Genome Analysis Toolkit’s (GATK) Best Practices (PMIDs, 20644199, 21478889, 25431634). To confirm the identified TBC1D24 variants direct Sanger sequencing was performed. The appropriate exon amplified by polymerase chain reaction (PCR) (primer sequences and PCR conditions on request) was directly sequenced by the Big Dye Terminator Cycle Sequencing System (Applied Biosystems Inc.) on an ABI PRISM 3730 DNA Analyzer (Applied Biosystems Inc.) and analyzed using Chromas (http://www.technelysium.com.au/chromas.html).

We present two siblings born to non-consanguineous parents of Polish descent. There is no significant family history.

The older sibling, A1, was diagnosed with cardiac arrhythmia antenatally, and was born via elective caesarean section at term. At the age of 5 weeks, his mother noted he had intermittent mouth-twitching movements while breastfeeding. This progressed to paroxysmal myoclonic twitching and jerking movements involving varying muscle groups, including those of his eyelids, face, lips, abdomen, and limbs. Myoclonic episodes ranged from short, spontaneously resolving tolerated events with small amplitude twitches to prolonged distressing events with larger amplitude jerks (Video 1A,B). He had preserved awareness with most episodes, but some prolonged episodes resulted in autonomic disturbance such as pallor, sweating, and reduced responsiveness. In casualty, prolonged episodes of myoclonus were often treated as status epilepticus. Benzodiazepines and rectal paraldehyde were reported to terminate some events. Although his symptoms were initially paroxysmal, by the age of 2 years he had almost constant myoclonus involving varying muscle groups. These symptoms were exacerbated by fatigue and abolished by sleep.

At the age of 10 months, A1 received a pacemaker for third-degree atrioventricular block. His development was delayed. He started walking unsteadily at 3 years and said his first word at 3 years of age. At 16 months of age, he was diagnosed with extreme hypermetropia. An early hearing screen was normal, but at the age of 5 years, he developed profound sensorineural hearing loss. On examination, he had dysplastic ears, downslanting palpebral fissures, silvery pigmentation to his hair, and a full philtrum. His weight was on the 25th centile and his head circumference was between the 9th and 25th centile. He had bilateral rotatory nystagmus. He had truncal hypotonia but increased peripheral tone, with a dynamic component, in all four limbs. Deep tendon reflexes were brisk in his lower limbs, with flexor plantar responses bilaterally. Asynchronous migratory myoclonus involving various muscle groups was easily observed throughout the examination.

Patient A2 had an unremarkable perinatal history. She started having myoclonic twitching and jerking in her limbs at the age of 6 weeks. Like her brother, this progressed to paroxysmal episodes of myoclonus, most often involving the abdomen or face. As she grew older, her myoclonus also became more widespread and constant.

A2 did not have cardiac symptoms. There have been no concerns regarding her vision or hearing. Currently, at the age of 3 years, she has poor balance and coordination in addition to speech delay. She does not have abnormal eye movements. She has normal tone and deep tendon reflexes.

Extensive neurometabolic investigations performed on blood, cerebrospinal fluid (CSF) and urine for both siblings revealed nothing of note apart from a mildly reduced CSF glucose on one occasion for A1 (1.9 mmol/l, plasma glucose 4.4 mmol/l) and two occasions for A2 (1.7 mmol/l, plasma 4.5 mmol/l; and 1.9 mmol/l, plasma 4.7 mmol/l). For both individuals, these normalized on repeat testing.

A1 had a normal male karyotype and normal microarray results. Testing for mutations in candidate genes for GLUT1 deficiency syndrome and mitochondrial disorders, including SLC2A1, POLG, and DGOUK, yielded negative results.

Repeated EEGs including prolonged EEGs encompassing sleep for both siblings showed a mild excess of slow activity, but no evidence of epileptiform activity. Polygraphic electromyogram (EMG) recordings of right and left deltoids, biceps, forearm, and quadriceps muscles demonstrated myoclonias of approximately 80–110 ms duration in all the EMG channels without any evidence of spread from one to another. A few myoclonias were more hypersynchronous, approximately 40–60 ms in duration (Supplementary Figure 2). Back-averaging did not reveal any preceding EEG change in either child. Nerve conduction studies and somatosensory evoked potential tests were normal.

A1 had serial cranial magnetic resonance imaging (MRI) scans from the age of 2 months to 19 months. These demonstrated hypoplasia of the frontal and temporal lobes. The deep grey matter appeared normal with no evidence of cortical dysplasia (Figure 1A). A computed tomography (CT) head scan showed tiny non-specific foci of calcification in the basal ganglia (Figure 1B).

Cranial MRI and MR spectroscopy performed at 6 weeks of age for A2 were normal. However, a repeat MRI scan at 3 years 10 months showed atrophy of the lateral aspects of the cerebellar hemispheres and symmetrical signaling abnormalities (Figure 1C).

A1 received trials of treatment with an extensive range of medication including anti-epileptics (valproate, carbamazepine, nitrazepam, levetiracetam, clobazam), metabolic supplements (coenzyme Q10, biotin, riboflavin, thiamine), levodopa, and piracetam. None of these achieved sustained benefit, although levetiracetam and clobazam each controlled myoclonus briefly. Immunotherapy had no significant effect.

Levetiracetam exacerbated A2’s symptoms and pyridoxine was ineffective. She did not tolerate the ketogenic diet. Bromocriptine resulted in dyskinetic movements, which terminated with discontinuation of the medication. Carbamazepine afforded her some symptomatic relief.

For both siblings as symptoms were abolished by sleep, the best therapeutic strategy seemed to be chloral hydrate used, as required, to induce sleep during periods of distress.

Variants identified through whole-exome sequencing were filtered by the following criteria: 1) very low frequency in control populations (exclusion of variants with a minor allele frequency > 0.1% in the established databases and 2,000 in-house analyzed exomes); 2) presentation of homozygous or compound heterozygous changes considering an autosomal recessive inheritance pattern; and 3) prediction of putative pathogenicity based on mutation type or in silico prediction of effects on protein function and/or structure. Using these criteria, two heterozygous variants confirmed by Sanger sequencing were identified in TBC1D24 (Supplementary Figure 1): 1) a previously reported missense change c.457G>A (p.Glu153Lys; rs376712059)6,13,15 and 2) a previously unreported frameshift mutation, c.545del (p.Thr182Serfs∗6) predicted to cause nonsense-mediated RNA decay or result in a truncated protein. Both mutations showed appropriate familial segregation.

Other possible disease-causing mutations identified in the two subjects that passed selection criteria were excluded (Supplementary Table 2). Mutations found in two genes (NOTCH4 and PRR21) could not be verified as it was not possible to design primers for confirmatory Sanger sequencing and segregation studies because of highly repetitive sequences. We note that whole-exome sequencing false-positive rates for indels can be as high as nearly 50%.19 Considering their phenotype, TBC1D24 was thus deemed to be the most likely candidate gene accounting for our patients’ symptoms.

Discussion

Myoclonus is rare and confirmation of a definitive diagnosis can often prove challenging. A definitive genetic diagnosis facilitates pre-pregnancy counseling and ends an often long diagnostic odyssey. Identification of causative genes can also contribute to the understanding of disease mechanisms and may facilitate development of novel targeted therapies. However, obtaining a genetic diagnosis is often complicated by genetic heterogeneity and phenotypic pleiotropy. Our report further illustrates how molecular genetic advances can facilitate gene discovery and clinical diagnosis.

TBC1D24 (OMIM 613577) encodes Tre2/Bub2/Cdc16 (TBC) 1 domain family member 24, a member of a family of Rab-specific GTPase-activating proteins.12 These have a role in coordinating Rab proteins and other GTPases for transport of intracellular vesicles. TBC1D24 interacts with ADP ribosylation factor 6 (ARF6), a GTPase with an essential role in membrane trafficking.5,20 The Rab GTPases control neuronal cell morphology and migration. In addition, TBC1D24 has a TBC lysine motif catalytic (TLDc) domain, thought to have a role in oxidative stress resistance.18,21 Loss of TBC1D24 function may result in abnormal vesicle trafficking, abnormal neuronal migration/maturation, and neurodegeneration.12,18,21

Mutations in TBC1D24 have been described in an array of disorders summarized in Table 1. Overall, among disorders associated with TBC1D24 mutations, recurring phenotypes include seizures, myoclonus, neurodevelopmental impairment, sensorineural hearing impairment, visual impairment, and cerebral and/or cerebellar atrophy on brain imaging. Movement disorders including dystonia, choreoathetosis, and dyskinesia have also been reported.12,13 Our sibship shares a number of clinical features with previously reported TBC1D24 cases. These include myoclonus, cerebellar atrophy, and neurodevelopmental impairment. A1 also had visual impairment and developed sensorineural hearing impairment.

To our knowledge, TBC1D24 mutations have not been reported in a phenotype involving prolonged, almost continuous multifocal myoclonus as the main presenting feature with no discernible epileptiform features on repeated interictal and ictal EEG recordings. Doummar et al.22 reported a case with similar multifocal myoclonus and homozygous c.809G>A (p.Arg270His) TBC1D24 mutations. However, unlike our sibship, interictal EEGs of this case presented paroxysmal epileptiform abnormalities and there was evidence suggesting his myoclonus had cortical origin. The myoclonia our sibship present with are more variable, asynchronous, and isolated, with a multifocal segmental pattern, than Doummar’s case, who had synchronous, generalized bursts of myoclonia. Interestingly, both siblings also had frequent abdominal myoclonus, which is rare and associated with myoclonus of spinal origin.

In conclusion, our report expands the TBC1D24 mutation spectrum by describing a novel mutation and extends the gene’s phenotypic spectrum. It suggests TBC1D24 should be considered amongst candidate genes in children with myoclonus and neurodevelopmental impairment even in the absence of clear epileptiform features.

Supplementary Material

All supplementary data referenced in this article is available here: http://dx.doi.org/10.7916/D8QN6CZG.

References

1. Lozsadi D. Myoclonus: a pragmatic approach. Pract Neurol 2012;12:215–224. doi: 10.1136/practneurol-2011-000107

2. Caviness JN, Alving LI, Maraganore DM, Black RA, McDonnell SK, Rocca WA. The incidence and prevalence of myoclonus in Olmsted County, Minnesota. Mayo Clin Proc 1999;74:565–569. doi: 10.4065/74.6.565

3. Zara F, Gennearo E, Stabile M, et al. Mapping of a locus for a familial autosomal recessive idiopathic recessive myoclonic epilepsy of infancy to chromosome 16p13. Am J Hum Genet 2000;66:1552–1557. doi: 10.1086/302876

4. de Falco FA, Majello L, Santangelo R, Stabile M, Bricarelli FD, Zara F. Familial infantile myoclonic epilepsy: clinical features in a large kindred with autosomal recessive inheritance. Epilepsia 2001;42:1541–1548. doi: 10.1046/j.1528-1157.2001.26701.x

5. Falace A, Filipello F, La Padula V, et al. TBC1D24, an ARF6-interacting protein, is mutated in familial infantile myoclonic epilepsy. Am J Hum Genet 2010;87:365–370. doi: 10.1016/j.ajhg.2010.07.020

6. Poulat AL, Ville D, de Bellescize J, et al. Homozygous TBC1D24 mutation in two siblings with familial infantile myoclonic epilepsy (FIME) and moderate intellectual disability. Epilepsy Res 2015;111:72–77. doi: 10.1016/j.eplepsyres.2015.01.008

7. Corbett MA, Bahlo M, Jolly L, et al. A focal epilepsy and intellectual disability syndrome is due to a mutation in TBC1D24. Am J Hum Genet 2010;87:371–375. doi: 10.1016/j.ajhg.2010.08.001

8. Afawi Z, Mandelstam S, Korczyn AD, et al. TBC1D24 mutation associated with focal epilepsy, cognitive impairment and a distinctive cerebro-cerebellar malformation. Epilepsy Res 2013;105: 240–244. doi: 10.1016/j.eplepsyres.2013.02.005

9. Milh M, Falace A, Villeneuve N, et al. Novel compound heterozygous mutations in TBC1D24 cause familial malignant migrating partial seizures of infancy. Hum Mutat 2013;34:869–872. doi: 10.1002/humu.22318

10. Duru N, Iseri SA, Selçuk N, Tolun A. Early-onset progressive myoclonic epilepsy with dystonia mapping to 16pter-p13.3. J Neurogenet 2010;24:207–215. doi: 10.3109/01677063.2010.514368

11. Guven A, Tolun A. TBC1D24 truncating mutation resulting in severe neurodegeneration. J Med Genet 2013;50:199–202. doi: 10.1136/jmedgenet-2012-101313

12. Stražišar BG, Neubauer D, Paro Panjan D, Writzl K. Early-onset epileptic encephalopathy with hearing loss in two siblings with TBC1D24 recessive mutations. Eur J Paediatr Neurol 2015;19:251–256. doi: 10.1016/j.ejpn.2014.12.011

13. Balestrini S, Milh M, Castiglioni C, et al. TBC1D24 genotype-phenotype correlation: Epilepsies and other neurologic features Neurology 2016;87:77–85. doi: 10.1212/WNL.0000000000002807

14. Rehman AU, Santos-Cortez RL, Morell RJ, et al. Mutations in TBC1D24, a gene associated with epilepsy, also cause nonsyndromic deafness DFNB86. Am J Hum Genet 2014;94:144–152. doi: 10.1016/j.ajhg.2013.12.004

15. Bakhchane A, Charif M, Salime S, et al. Recessive TBC1D24 mutations are frequent in Moroccan non-syndromic hearing loss pedigrees. PLoS ONE 2015;10:e0138072. doi: 10.1371/journal.pone.0138072

16. Azaiez H, Booth KT, Bu F, et al. TBC1D24 mutation causes autosomal-dominant nonsyndromic hearing loss. Hum Mutat 2014;35:819–823. doi: 10.1002/humu.22557

17. Zhang L, Hu L, Chai Y, Pang X, Yang T, Wu H. A dominant mutation in the stereocilia-expressing gene TBC1D24 is a probable cause for nonsyndromic hearing impairment. Hum Mutat 2014;35:814–818. doi: 10.1002/humu.22558

18. Campeau PM, Kasperaviciute D, Lu JT, et al. The genetic basis of DOORS syndrome: an exome-sequencing study. Lancet Neurol 2014;13:44–58. doi: 10.1016/S1474-4422(13)70265-5

19. Belkadi A, Bolze A, Itan Y, et al. Whole-genome sequencing is more powerful than whole-exome sequencing for detecting exome variants. Proc Natl Acad Sci USA 2015;112:5473–5478. doi: 10.1073/pnas.1418631112

20. Falace A, Buhler E, Fadda M, et al. TBC1D24 regulates neuronal migration and maturation through modulation of the ARF-6 dependent pathway. Proc Natl Acad Sci USA 2014;111:2337–2342. doi: 10.1073/pnas.1316294111

21. Finelli MJ, Sanchez-Pulido L, Liu KX, et al. The evolutionarily conserved Tre2/Bub2/Cdc16 (TBC), lysin motif (LysM), domain catalytic (TLDc) domain is neuroprotective against oxidative stress. J Biol Chem 2016;291:2751–2763. doi: 10.1074/jbc.M115.685222

22. Doummar D, Mignot C, Apartis E, et al. A novel homozygous TBC1D24 mutation causing multifocal myoclonus with cerebellar involvement. Mov Disord 2015;30:1431–1432. doi: 10.1002/mds.26303

Table 1. Phenotypes Associated with TBC1D24 Mutations

Clinical Phenotype Familial Infantile
Myoclonic Epilepsy
(OMIM 605021)
Focal Epilepsy with
Cerebrocerebellar
Malformation
MMPSI
(OMIM 615338)
Progressive Myoclonic
Epilepsy with Dystonia
(OMIM 615338)
EOEE and Hearing
Loss
References Zara et al.3,
de Falco et al.4,
Falace et al.5, Poulat et al.6
Corbett et al.7,
Afawi et al.8
Milh et al.9 Duru et al.10,
Guven and Tolun11
Stražišar et al.12
Reported
mutations/
genotype
c.439G>C (p.Asp147His)
c.1526C>T (p.Ala509Val)
c.457G>A (p.Glu157Lys)
c.751C>T (p.Phe251Leu) c.468C>A (p.Cys156∗)
c.686T>A (p.Phe229Ser)
c.969_970delGT
(p.Ser324Thrfs∗3)
c.32A>G (p.Asp11Gly)
c.1008delT
(p.His336GInfs∗12)
Inheritance AR AR AR AR AR
Clinical features Seizures Normal
psychomotor development
and neurological
examination to moderate
intellectual and
psychomotor impairment
Bulbous nose and flat nasal
root
Seizures
Myoclonus
Moderate intellectual
disability
Ataxic with cerebellar
signs
Dystonia
Dysarthria
Seizures
Psychomotor regression
Axial hypotonia
Loss of visual contact
Seizures
Post-ictal hemiparesis
Dystonic episodes
Myoclonus with startle
responses to auditory and
tactile stimuli
Axial hypotonia
Pyramidal signs
Severe neurodevelopmental
impairment
Vulnerability to infection
Bilateral optic atrophy,
macular degeneration and
visual impairment in one individual
Seizures
Profound sensorineural
deafness
Myoclonic jerks
Acquired microcephaly
Dyskinetic movements
Axial hypotonia
Poor visual contact
Types of seizures GTC Myoclonic: trigger sensitive Focal seizures with auras
Tonic–clonic
Myoclonic
Focal prolonged migrating
clonic seizures
Focal/unilateral
Clonic seizures
Myoclonic
Tonic
Clonic seizures
Tonic seizures
EEG/EMG
findings
Preserved background.
1 individual with slow
background activity in
occipital region. Interictal
multiple diffuse spikes and
slow waves. Ictal EEG
with low amplitude spikes
at vertex Jerk-locked back
averaging confirmed
cortical myoclonus
Slow background rhythms.
No epileptiform
discharges. Ictal EEG not
available
Focal migrating EEG
discharges during seizures
Interictal EEG:
disorganized
Slow background in EEG
Multifocal or bilateral
generalized multiple spikes and
spike waves in EEG associated
with myoclonias.
Generalized spike-wave
discharges with frontocentral
predominance during seizures
No clear EEG correlate for
myoclonic jerks
Imaging findings Normal 1 individual with
nodular periventricular
heterotopia 1 individual
had MRI abnormalities in
lentiform nuclei,
ventricular dilatation and
white matter changes
post-cardiac arrest. An
earlier MRI was normal
Selective atrophy and
signal abnormality in
cerebellum
Cerebral cortical
thickening most marked in
cingulate regions and
occipital poles
Global cerebral atrophy
sparing the posterior fossa
Thin corpus callosum
Delayed myelination
Diffuse cerebral atrophy
(asymmetrical for one patient)
Cerebellar atrophy
Prominent frontotemporal
atrophy
Clinical Phenotype Spectrum of Epilepsy
Phenotypes Including
DOORS Syndrome
DOORS Syndrome
(OMIM 220500)
Non-syndromic
Deafness (DFNB86)
(OMIM 614617)
Non-syndromic
Hearing Loss (DFNA65)
(OMIM 616044)
Migrating
Paroxysmal
Myoclonus and
Cerebellar Signs

Abbreviations: AD, Autosomal Dominant; AR, Autosomal Recessive; ASD, Atrial Septal Defect; EEG, Electroencephalogram; EOEE, Early-onset Epileptic Encephalopathy; GTC, Generalized Tonic Clonic; MMPSI, Malignant Migrating Partial Seizures of Infancy; NA, Not Available; VSD, Ventricular Septal Defect.

References Balastrini et al.13 Campeau et al.18 Rehman et al.14,
Bakhchane et al.15
Azaiez et al.16,
Zhang et al.17
Doummar et al.22
Reported
mutations/genotype
c.32A>G (p.Asp11Gly)
c.58C>T (p.Gln20∗)
c.115G>C (p.Ala39Pro)
c.118C>T (p.Arg40Cys)
c.119G>T (p.Arg40Leu)
c.277C>T (p.Pro93Ser)
c.313T>C (p.Cys105Arg)
c.328G>A (p.Gly110Ser)
c.439G>C (p.Asp147His)
c.457G>A (p.Glu153Lys)
c.468C>A (p.Cys156∗)
c.533C>G (p.Ser178Trp)
c.619C>T (p.Gln207∗)
c.679C>T (p.Arg227Trp)
c.680G>A (p.Arg227Gln)
c.686T>C (p.Phe229Ser)
c.724C>T (p.Arg242Cys)
c.731C>T (p.Ala244Val)
c.751T>C (p.Phe251Leu)
c.809G>A (p.Arg270His)
c.845C>G (p.Pro282Arg)
c.919A>G (p.Asn307Asp)
c.957G>C (p.Lys319Asn)
c.969_970delGT(p.Ser324Thrfs∗3)
c.999G>T (p.Leu333Phe)
c.1008delT (p.His336Glnfs∗12)
c.1126G>C (p.Gly376Arg)
c.1384del (p.Glu462Serfs∗61)
c.1460dup (p.His487Glnfs∗71)
c.1079G>T (p.Arg360Leu)
c.1499C>T (p.Ala500Val)
c.1544C>T (p.Ala515Val)
c.1661_1667del (p.Gln554Leufs∗12)
c.724C>T (p.Arg242Cys)
c.118C>T (p.Arg40Cys)
c.119G>T (p.Arg40Leu)
c.1008delT (p.His336GInfs∗12)
c.1206+5G>A (Splice site)
c.58C>G (p.Gln20Glu)
c.328G>A (p.Gly110Ser)
c.999G>T (p.Leu333Phe)
c.208G>T (p.Asp70Tyr)
c.878G>C (p.Arg293Pro)
c.641G>A (p.Arg214His)
c.1316insG (p.Val439Valfs∗32)
c.457G>A (p.Glu153Lys)
c.798G>T (p.Lys266Asn)
c.533C>T (p.Ser178Leu) c.809G>A (p.Arg270His)
Inheritance AR AR AR AD AR
Clinical features Seizures
In some
  Axial hypotonia
  Acquired microcephaly
  Poor visual contact, cortical
  blindness, bilateral optic
  atrophy, macular degeneration
  Sensorineural deafness
  Dysmorphia including
  bulbous nose with flat nasal
  root, thin or prominent
  philtrum, synophrys, up or
  down slanting palpebral fissures
  Acral abnormalities:
  hypoplastic terminal
  phalanges, brachydactyly
  Skeletal abnormalities tibial
  torsion, scoliosis, etc.
  Movement disorders: dystonic
  episodes, tremor, dyskinesia
  Ataxia
  Feeding difficulties
  Heart defects
   Autism spectrum disorder
  Pyschosis
   Hyperactivity
  Peripheral neuropathy
  Renal anomalies
Seizures
Sensorineural deafness
Small or absent nails
Hypoplastic terminal
phalanges
2-Oxoglutaric aciduria
Neurodevelopmental
Impairment
Bulbous nose with flat
nasal root
In some individuals:
   Microcephaly in
   one-third
   Occasional
   craniosynostosis
   Autistic spectrum
  disorder
  Eyes: colobomas,
   visual impairment
   Heart defects (ASD/
  VSD), double outlet
   right ventricle)
   Kidneys, adrenal glands,
   and genitalia
  malformations
Non-syndromic sensorineural
deafness
Of 15 affected individuals
assessed for epilepsy in
Rehman et al.16,
1 individual had a history
of seizures: attributed to
coincidence
Family history of epilepsy
Non-syndromic hearing
loss with onset in the third decade
Paroxysmal migrating
myoclonus with preserved
awareness
Ataxia
Progressive cognitive
decline
Types of
seizures
Infantile spasms
Febrile seizures
Myoclonic
Tonic seizures
Clonic seizures
Tonic–clonic with/without
focal onset
Focal seizures
GTC
Myoclonic
Infantile spasms
Absence seizures
Focal seizures
Not mentioned NA NIL
EEG/EMG
findings
Focal epileptiform discharges:
frontocentral, temporal,
occipital
Multifocal discharges
Migrating focal discharges
Generalized spike-waves
Not mentioned Normal Not done Interictal EEG: slow waves
in occipital region
Imaging findings Cerebellar atrophy
Global cerebral atrophy
Cerebral atrophy sparing the
posterior fossa
Hippocampal atrophy
Basal ganglia atrophy
Hippocampal sclerosis
Delayed myelination
Thin corpus callosum
Hyperintensity of basal ganglia
Hyperintensity in cerebellar
cortex and white matter
Thin corpus callosum
Corpus callosum agenesis
Dandy walker
malformation
Cerebellar atrophy
Hyperintense T2 in
cerebellar hemispheres
Cortical atrophy
Delayed myeliniation
Increased T2 signal in
frontal region
Increased flair in occipital horn
Normal Not mentioned Progressive hemispheric
cerebellar atrophy with
hypersignal of the
cerebellar cortex and
white matter on T2 and
fluid-attenuated inversion
recovery sequences

Video 1A. Patient A1 at various ages. The video demonstrates orolingual and facial myoclonus.

Video 1B. Patient A1 at various ages. The video demonstrates limb myoclonus, abdominal myoclonus and widespread polymyoclonus. Towards the end of the video distal choreoathetoid movements are also present in the upper limbs.

Video 1C. Patient A2 at approximately 3 months of age. The video demonstrates myoclonus in the right arm and orolingual myoclonus.

Figure 1. Magnetic Resonance Imaging Features in Sibship with TBC1D24 Mutations. (A) MRI brain scan (Axial T2-weighted) of A1 age 19 months showing underdevelopment of the frontal and temporal lobes. (B) CT head scan of A1 20 months showing small non-specific foci of calcification within the basal ganglia. (C) MRI head scan (Coronal T2-weighted) of A2 at 3 years 10 months showing symmetrical signal abnormalities and atrophy of the lateral aspects of the cerebellar hemispheres.

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