Coffin-Lowry syndrome in Chinese

Am J Med Genet A. 2019 Oct;179(10):2043-2048. doi: 10.1002/ajmg.a.61323. Epub 2019 Aug 9.

Abstract

Coffin-Lowry syndrome (CLS) is a well-described syndrome characterized by intellectual disability, growth retardation, recognizable dysmorphic features, and skeletal changes. It is an X-linked syndrome where males are more severely affected and females have high variability in clinical presentations. This case series reports nine molecularly confirmed Chinese CLS patients from six unrelated families (three with familial variants and three with de novo variants). There is a wide genotypic spectrum with five novel variants in RPS6KA3 gene. Clinical phenotype and facial features of these Chinese CLS patients are comparable to what has been described in other ethnicities.

Keywords: RPS6KA3; Chinese; Coffin-Lowry syndrome.

Publication types

  • Case Reports

MeSH terms

  • Asian Continental Ancestry Group / genetics*
  • Coffin-Lowry Syndrome / genetics*
  • Family
  • Female
  • Genotype
  • Humans
  • Male
  • Pedigree
  • Phenotype