FTO variant associated with malformation syndrome

Am J Med Genet A. 2016 Apr;170A(4):1023-8. doi: 10.1002/ajmg.a.37515. Epub 2015 Dec 24.

Abstract

Common FTO variants are associated with obesity. However, it has recently been shown that homozygous FTO c.947G>A variant, which predicts p.R316Q, and c.956C>T, which predicts p.S319F, are associated with a malformation syndrome inherited in an autosomal recessive pattern. We present a similar homozygous FTO c.965G>A variant that predicts p.R322Q, associated with a lethal malformation syndrome in a consanguineous Yemeni family. Functional studies showed that the p.R316Q, p.S219F, and p.R322Q variants render the FTO protein inactive. We further expand on the phenotype of homozygous FTO loss-of-function mutations to include eye abnormalities, gingival overgrowth, craniosynostosis, and cutaneous photosensitivity.

Keywords: exome sequencing; fat mass-and obesity-associated gene (FTO); multiple congenital anomalies; variant mutation.

Publication types

  • Case Reports

MeSH terms

  • Abnormalities, Multiple / diagnosis*
  • Abnormalities, Multiple / genetics*
  • Alleles
  • Alpha-Ketoglutarate-Dependent Dioxygenase FTO / genetics*
  • Brain / pathology
  • Female
  • Genetic Variation*
  • Homozygote
  • Humans
  • Infant
  • Male
  • Mutation
  • Phenotype*
  • Syndrome
  • Tomography, X-Ray Computed

Substances

  • Alpha-Ketoglutarate-Dependent Dioxygenase FTO
  • FTO protein, human