Ibnosina Journal of Medicine and Biomedical Sciences

CASE REPORT
Year
: 2019  |  Volume : 11  |  Issue : 4  |  Page : 192--195

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


Waseem Mahmoud Fathalla1, Farah Hussein Salman2 
1 Division of Pediatric Neurology, Department of Pediatrics, Mafraq Hospital, Abu Dhabi, UAE
2 Department of Pediatrics, Sheikh Khalifa Medical City, Abu Dhabi, UAE

Correspondence Address:
Waseem Mahmoud Fathalla
Department of Pediatrics, Division of Pediatric Neurology, Mafraq Hospital, PO Box: 2951, Abu Dhabi
UAE

“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.


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;11:192-195


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 2020 Apr 6 ];11:192-195
Available from: http://www.ijmbs.org/article.asp?issn=1947-489X;year=2019;volume=11;issue=4;spage=192;epage=195;aulast=Fathalla;type=0