Human Genome Variation (Aug 2021)

Intellectual disability and microcephaly associated with a novel CHAMP1 mutation

  • Yuta Asakura,
  • Hitoshi Osaka,
  • Hiromi Aoi,
  • Takeshi Mizuguchi,
  • Naomichi Matsumoto,
  • Takanori Yamagata

DOI
https://doi.org/10.1038/s41439-021-00165-7
Journal volume & issue
Vol. 8, no. 1
pp. 1 – 3

Abstract

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Abstract Mutations in a number of genes related to chromosomal segregation reportedly cause developmental disorders, e.g., chromosome alignment-maintaining phosphoprotein 1 (CHAMP1). We report on an 8-year-old Japanese girl who presented with a developmental disorder and microcephaly and carries a novel nonsense mutation in CHAMP1. Therefore, CHAMP1 mutation should be considered as a differential diagnosis of global developmental delay and microcephaly.