Malan syndrome has recently been characterized to present Sotos-like phenotypes, such as intellectual disability and macrocephaly, with mutations in the gene. Herein, we report a 38-year-old patient with a novel single adenine insertion mutation in exon 2 of the 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.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5451486 | PMC |
http://dx.doi.org/10.1038/hgv.2017.22 | DOI Listing |
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