| Literature DB >> 28584646 |
Tsukasa Oshima1, Hironori Hara1, Norifumi Takeda1, Eriko Hasumi1, Yukiko Kuroda2, Go Taniguchi3, Ryo Inuzuka2, Kan Nawata4, Hiroyuki Morita1, Issei Komuro1.
Abstract
Malan syndrome has recently been characterized to present Sotos-like phenotypes, such as intellectual disability and macrocephaly, with mutations in the NFIX gene. Herein, we report a 38-year-old patient with a novel single adenine insertion mutation in exon 2 of the NFIX gene (c.290_291insA). He developed early-onset thoracic aortic aneurysm and dissection, which was a rare complication but deserves particular attention in relatively long-lived patients with Sotos-like phenotypes.Entities:
Year: 2017 PMID: 28584646 PMCID: PMC5451486 DOI: 10.1038/hgv.2017.22
Source DB: PubMed Journal: Hum Genome Var ISSN: 2054-345X