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 Table of Contents  
Year : 2019  |  Volume : 11  |  Issue : 4  |  Page : 192-195

“Neurodevelopmental disorder with microcephaly, epilepsy, and brain atrophy” with a novel mutation

1 Division of Pediatric Neurology, Department of Pediatrics, Mafraq Hospital, Abu Dhabi, UAE
2 Department of Pediatrics, Sheikh Khalifa Medical City, Abu Dhabi, UAE

Date of Submission28-Sep-2019
Date of Decision25-Nov-2019
Date of Acceptance25-Nov-2019
Date of Web Publication30-Dec-2019

Correspondence Address:
Waseem Mahmoud Fathalla
Department of Pediatrics, Division of Pediatric Neurology, Mafraq Hospital, PO Box: 2951, Abu Dhabi
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Source of Support: None, Conflict of Interest: None

DOI: 10.4103/ijmbs.ijmbs_61_19

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“Neurodevelopmental disorder with microcephaly, epilepsy, and brain atrophy” is a newly described disorder related to homozygous mutations in TRAPPC6B gene. Although nonspecific, the features of this disorder appear to have a characteristic course of postnatal progressive microcephaly that should raise the suspicion of this disorder. To the best of our knowledge, only eight cases were published in the literature. Here, we report a new case with a novel mutation and compare the clinical findings to the published cases. This case was not picked up by whole-exome sequencing but rather by whole-genome sequencing, emphasizing the importance of pursuing an etiological diagnosis in patients with otherwise unexplained progressive neurological disorders.

Keywords: Brain atrophy, epilepsy, neurodevelopmental disorder with microcephaly

How to cite this article:
Fathalla WM, Salman FH. “Neurodevelopmental disorder with microcephaly, epilepsy, and brain atrophy” with a novel mutation. Ibnosina J Med Biomed Sci 2019;11:192-5

How to cite this URL:
Fathalla WM, Salman FH. “Neurodevelopmental disorder with microcephaly, epilepsy, and brain atrophy” with a novel mutation. Ibnosina J Med Biomed Sci [serial online] 2019 [cited 2021 Dec 1];11:192-5. Available from: http://www.ijmbs.org/text.asp?2019/11/4/192/274310

  Introduction Top

Neurodevelopmental disorder with microcephaly, epilepsy, and brain atrophy (NEDMEBA) OMIM# 617862 is a recently described disorder associated with autosomal-recessive intellectual disability.[1],[2] Global developmental delay is a common disorder, affecting about 1%–3% of children.[3] Routine cytogenetic testing has been recommended even in the absence of dysmorphic features since the diagnostic yield is as high as 3.5%–10%.[3] However, the development of clinical whole-exome and whole-genome sequencing (WGS) has further increased the diagnostic yield of genetic studies[4],[5] in addition to enabling the identification of new genetic mutations not previously linked to clinical disorders.[5],[6] Recently, Marin-Valencia et al. first described a new disorder of “autosomal-recessive NEDMEBA associated with homozygous mutations in TRAPPC6B gene in six children from three unrelated consanguineous families from different parts of Egypt and performed functional studies on the mutations providing evidence of the role of TRAPPC6B gene dysfunction to the phenotype.[1] We report a new case of this rare genetic cause of developmental delay with microcephaly, epilepsy, and brain atrophy related to a novel intronic homozygous mutation in TRAPPC6B gene. We aim to reaffirm the phenotypic spectrum of this disorder, as well as raise awareness about this condition in children with otherwise unexplained neurodevelopmental disorder with comorbidities.

  Case Report Top

A 5-year-old Pakistani male with neurodevelopmental delay and severe intellectual disability was referred to our clinic for the evaluation due to reported neonatal seizures and “perinatal complications.” The patient was the product of full-term gestation through normal vaginal delivery with a birth weight of 3.5 kg (50 percentile), length of 51 cm (69 percentile), and head circumference of 33 cm (6.5 percentile). Parents are consanguineous. At 5 years of age, he has no language development except for monosyllabic sounds (Ma, Da), he does not understand simple commands, he recognizes his parents but has poor social interaction, and is hyperactive while awake with nonpurposeful nonstereotypic head, hand, and leg movements. He can sit from the supine position but cannot stand or walk.

Physical examination revealed an alert child who is not oriented, has dysmorphic facial features, including progressive microcephaly, almond-shaped eyes, in addition to inverted wide-spaced nipples [Figure 1], lower abdomen wall fat pads, and long thumbs. The heart, lungs, abdomen, and genitourinary examination are unremarkable. His neurological examination is remarkable for axial and limb hypotonia, markedly diminished deep-tendon reflexes, and inability to stand or take steps.
Figure 1: Microcephaly with mild retrognathia, prominent ears, almond-shaped eyes, wide-spaced nipples, and fat pads

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Magnetic resonance imaging (MRI) of the brain [Figure 2] revealed a thin corpus callosum with periventricular and deep white matter signal hyperintensity reported to be “suggestive of perinatal hypoxic-ischemic changes;” however, there was no substantiated evidence of hypoxia/ischemia at birth. Nerve conduction study was normal for age; however, his EMG revealed nonspecific chronic neurogenic features. A metabolic screen, including plasma amino acids, urine organic acids, plasma acylcarnitine, leukocyte lysosomal enzymes as well as mucopolysacchride screen was within normal for age. Prader-Willi fluorescence in situ hybridization probe was negative. Based on the negative initial investigations, whole-exome sequencing (WES) was performed and was reported as negative. However, WGS identified a homozygous likely pathogenic variant c. 149 + 2T >A in Intron 2 in the TRAPPC6B gene, which is consistent with the genetic diagnosis of “autosomal recessive NEDMEBA.” This variant was found on the WES but not reported at the time due to lack of clinical reports of its pathogenic significance. The revaluation of parents previous WES has confirmed their carrier status.
Figure 2: Brain magnetic resonance imaging showing thin corpus callosum (white arrow sagittal view), and periventricular hyperintense T2 signal on axial FLAIR, as well as an external capsule (red arrows) hyperintense T2 signals

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  Discussion Top

Pathology and genetics

TRAPPC6B gene codes the β subunit of transport protein particle (TRAPP) protein C6, which is part of the TRAPP complex involved in tethering mechanism involved in vesicle transport.[7] Kümmel et al. speculate that the TPC6 and BET3 (another TRAPP subunit) interact to form anin vivo subcomplex that could represent the starting point for complex assembly at the Golgi membrane.[7] Harripaul et al. reported loss-of-function mutations in TRAPPC6B among nine new autosomal recessive intellectual disability genes[2] and have noted that these genes are highly expressed in the prenatal brain. It is logical to speculate that the function of TRAPPC6B as part of TRAPP complex and its role in vesicle transport are critical to cell trafficking during the critical period of brain development. However, Marin-Valencia et al. reported that fibroblasts from affected patients did not show any obvious abnormalities in the Golgi apparatus, but the expression studies in knock out zebrafish model showed decreased cell survival and increased number of apoptotic cells.[1] This may well correlate with some of the clinical features of the microcephaly and thin corpus callosum.

Clinical features

NEDMEBA is a neurodevelopmental disorder associated with microcephaly, epilepsy, and brain atrophy. The main clinical features involve the central nervous system, psychomotor development, and growth.

Dysmorphology and extra-neurological involvement

No frank dysmorphic features are reported with this condition. However, we observed that the patient described here does have prominent ears, almond-shaped eyes, inverted wide-spaced nipples, and relatively long thumbs. Marin-Valencia et al. reported prominent ears in their cohort but attributed that to the microcephaly. The main extra-neurological manifestation is strabismus.

Neurological manifestations

Progressive microcephaly is an important clinical feature reported in all cases. These children also manifest severe intellectual disability, lack of speech development, epilepsy, autistic features, hypotonia, and ataxia. Our patient did not manifest any seizures yet, although he had undocumented report of “neonatal convulsions.” His most prominent neurological manifestations are the lack of speech and significant hypotonia/ataxia.

Brain imaging

Brain MRI revealed a thin corpus callosum, cortical atrophy, brainstem, and cerebellar atrophy. These findings worsened overtime on repeated brain imaging in some of the patients.[1] The patient, in this case, did not undergo repeat imaging due to no clinical indication. In this case, however, abnormal T2 hyperintensities in the deep white matter were also present, suggesting the MRI abnormalities in patients with TRAPPC6B mutations may have a wider spectrum of neuroradiological abnormalities than earlier reported.


To date, all eight published cases, six by Marin-Valencia et al. and two by Harripaul et al., were diagnosed by WES,[1],[2] suggesting that the clinical features are relatively nonspecific. Another recently published case by Nair et al.[8] was also diagnosed by WES showing a homozygous likely pathogenic c. 23T >A variant in exon 1. The case reported here shows a phenotypic expression and clinical course very consistent with the published cases, specifically the postnatal progressive microcephaly and thin corpus callosum and brain atrophy [Table 1]. It is probably too early in the course of discovery of this disorder to recommend single gene testing as the clinical phenotype may later prove to be genetically heterogeneous. Moreover, this patient showed an intronic mutation that could be missed on WES. Hence, we suggest that WGS may be the most appropriate diagnostic tool in children with a compatible clinical picture who otherwise do not have an etiological diagnosis for their progressive postnatal microcephaly, intellectual disability, and lack of speech development.
Table 1: Comparison of clinical and diagnostic features of the present case and previous published case series

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There is no known specific treatment at this stage. The management is symptomatic and supportive with focus on early intervention.


Patients should be followed up for growth failure, progressive motor difficulties, strabismus, as well as autistic spectrum disorder. Parents should be offered testing for heterozygous status to inform the risk of recurrence in future pregnancies.


As a relatively new neurodegenerative disorder, it remains unclear what the long-term outcome of these children is likely to be, although the early manifestation of severe progressive microcephaly and intellectual disability indicate a high risk for continued regression and long-term disability.

Declaration of patient consent

The authors certify that they have obtained all appropriate patient consent forms. In the form, the patient's guardian has given his consent for patient's images and other clinical information to be reported in the journal. He understands that name and initial will not be published and due efforts will be made to conceal their identity, but anonymity cannot be guaranteed.

Authors' contributions

Both authors contributed to the preparation, revision, and approval of the final version.

Financial support and sponsorship


Conflicts of interest

There are no conflicts of interest.

Compliance with ethical principles

A written consent was obtained from the father for photographs and reporting the case.

  References Top

Marin-Valencia I, Novarino G, Johansen A, Rosti B, Issa MY, Musaev D, et al. A homozygous founder mutation in TRAPPC6B associates with a neurodevelopmental disorder characterised by microcephaly, epilepsy and autistic features. J Med Genet 2018;55:48-54.  Back to cited text no. 1
Harripaul R, Vasli N, Mikhailov A, Rafiq MA, Mittal K, Windpassinger C, et al. Mapping autosomal recessive intellectual disability: Combined microarray and exome sequencing identifies 26 novel candidate genes in 192 consanguineous families. Mol Psychiatry 2018;23:973-84.  Back to cited text no. 2
Shevell M, Ashwal S, Donley D, Flint J, Gingold M, Hirtz D, et al. Practice parameter: Evaluation of the child with global developmental delay: Report of the Quality Standards Subcommittee of the American Academy of Neurology and The Practice Committee of the Child Neurology Society. Neurology 2003;60:367-80.  Back to cited text no. 3
Yavarna T, Al-Dewik N, Al-Mureikhi M, Ali R, Al-Mesaifri F, Mahmoud L, et al. High diagnostic yield of clinical exome sequencing in Middle Eastern patients with Mendelian disorders. Hum Genet 2015;134:967-80.  Back to cited text no. 4
Charng WL, Karaca E, Coban Akdemir Z, Gambin T, Atik MM, Gu S, et al. Exome sequencing in mostly consanguineous Arab families with neurologic disease provides a high potential molecular diagnosis rate. BMC Med Genomics 2016;9:42.  Back to cited text no. 5
Alazami AM, Patel N, Shamseldin HE, Anazi S, Al-Dosari MS, Alzahrani F, et al. Accelerating novel candidate gene discovery in neurogenetic disorders via whole-exome sequencing of prescreened multiplex consanguineous families. Cell Rep 2015;10:148-61.  Back to cited text no. 6
Kümmel D, Müller JJ, Roske Y, Misselwitz R, Büssow K, Heinemann U. The structure of the TRAPP subunit TPC6 suggests a model for a TRAPP subcomplex. EMBO Rep 2005;6:787-93.  Back to cited text no. 7
Nair P, El-Bazzal L, Mansour H, Sabbagh S, Al-Ali MT, Gambarini A, et al. Further delineation of the TRAPPC6B disorder: Report on a new family and review. J Pediatr Genet 2019;8:252-6.  Back to cited text no. 8


  [Figure 1], [Figure 2]

  [Table 1]


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