| Literature DB >> 27000257 |
Nuha Alrayes1, Hussein Sheikh Ali Mohamoud2, Saleem Ahmed3, Mona Mohammad Almramhi4, Taghreed Mohammad Shuaib5, Jun Wang6, Jumana Yousuf Al-Aama7, Kate Everett2, Jamal Nasir2, Musharraf Jelani8.
Abstract
Autosomal recessive primary microcephaly (MCPH) refers to a genetically heterogeneous group of neurodevelopmental disorders in which patients exhibit a marked decrease in occipitofrontal head circumference at birth and a variable degree of intellectual disability. To date, 18 genes have been reported for MCPH worldwide. We enrolled a consanguineous family from Saudi Arabia presenting with primary microcephaly, developmental delay, short stature and intellectual disability. Whole exome sequencing (WES) with 100× coverage was performed on two affected siblings after defining common regions of homozygosity through genome-wide single nucleotide polymorphism (SNP) microarray genotyping. WES data analysis, confirmed by subsequent Sanger sequence validation, identified a novel homozygous deletion mutation (c.967delA; p.Glu324Lysfs12*) in exon 10 of the alkylglycerol monooxygenase (AGMO) gene on chromosome 7p21.2. Population screening of 178 ethnically matched control chromosomes and consultation of the Exome Aggregation Consortium database, containing 60,706 individuals' exomes worldwide, confirmed that this mutation was not present outside the family. To the best of our knowledge, this is the first evidence of an AGMO mutation underlying primary microcephaly and intellectual disability in humans. Our findings further expand the genetic heterogeneity of MCPH in familial cases.Entities:
Keywords: Alkylglycerol monooxygenase; Autosomal recessive primary microcephaly; Frameshift deletion mutation; Novel homozygous; Saudi Arabia; Whole exome sequencing
Mesh:
Substances:
Year: 2016 PMID: 27000257 DOI: 10.1016/j.jns.2016.02.063
Source DB: PubMed Journal: J Neurol Sci ISSN: 0022-510X Impact factor: 3.181