MIRAGE syndrome caused by a novel missense variant (p.Ala1479Ser) in the SAMD9 gene

Abstract

MIRAGE syndrome is a recently identified disorder characterized by myelodysplasia, infection, restriction of growth, adrenal hypoplasia, genital phenotypes, and enteropathy. It is caused by a gain-of-function variant in the <i>SAMD9</i> gene, but there is limited knowledge regarding the genotype-phenotype correlation. We herein report a Japanese patient with MIRAGE syndrome carrying a novel de novo heterozygous missense variant in the <i>SAMD9</i> gene (c.4435 G > T; p.Ala1479Ser).