Allelic heterogeneity in a patient with postzygotic MTOR-related hypomelanosis of Ito with neurodevelopmental abnormalities

Clin Genet. 2024 May;105(5):581-583. doi: 10.1111/cge.14511. Epub 2024 Feb 20.

Abstract

A case of mosaic MTOR-associated hemimegalencephaly and hypomelanosis of Ito, died at 33 probably because of sudden unexpected death in epilepsy. Assessment of the variant allele fraction (VAF) in different tissues postmortem showed high variability not correlated with clinical features, representing the most detailed assessment of VAFs in different tissues to date.

Keywords: MTOR; SUDEP; hemimegalencephaly; hypomelanosis of Ito; neurodevelopmental disorder.

Publication types

  • Case Reports

MeSH terms

  • Alleles
  • Autopsy
  • Humans
  • Hypopigmentation* / genetics
  • TOR Serine-Threonine Kinases

Substances

  • TOR Serine-Threonine Kinases
  • MTOR protein, human