UBE2A UBE2A deficiency in two siblings: A novel splicing variant inherited from a maternal germline mosaicism

摘要

UBE2A deficiency is a syndromic condition of X‐linked intellectual disability (ID) characterized by typical dysmorphic features that include synophrys, prominent supraorbital ridges, almond‐shaped, and deep‐set eyes, large ears, wide mouth, myxedematous appearance, hirsutism, micropenis, and onychodystrophy. To date, only seven familial UBE2A intragenic mutations and nine larger microdeletions encompassing UBE2A have been reported. Here, we describe two siblings with X‐linked ID and typical clinical features of UBE2A deficiency caused by a novel hemizygous variant, identified by massively parallel sequencing of X‐exome. The synonymous c.330GA substitution in UBE2A modifies the last nucleotide of exon 5, causing the exon skipping and resulting in an out‐of‐frame transcript, likely encoding for a truncated form of the ubiquitin‐conjugating enzyme E2 A. As confirmed by deep sequencing, the c.330GA substitution in UBE2A was undetectable in genomic DNA from maternal blood cells, suggesting that the recurrent UBE2A deficiency observed in males of this family is caused by a maternal germline mosaicism.