NHS Gene Mutations in Ashkenazi Jewish Families with Nance-Horan Syndrome

Curr Eye Res. 2017 Sep;42(9):1240-1244. doi: 10.1080/02713683.2017.1304560. Epub 2017 May 30.

Abstract

Purpose: To describe ocular and extraocular abnormalities in two Ashkenazi Jewish families with infantile cataract and X-linked inheritance, and to identify their underlying mutations.

Methods: Seven affected members were recruited. Medical history, clinical findings, and biometric measurements were recorded. Mutation analysis of the Nance-Horan syndrome (NHS) gene was performed by direct sequencing of polymerase chain reaction-amplified exons.

Results: An unusual anterior Y-sutural cataract was documented in the affected male proband. Other clinical features among examined patients included microcorneas, long and narrow faces, and current or previous dental anomalies. A nonsense mutation was identified in each family, including a previously described 742 C>T, p.(Arg248*) mutation in Family A, and a novel mutation 2915 C>A, p.(Ser972*) in Family B.

Conclusions: Our study expands the repertoire of NHS mutations and the related phenotype, including newly described anterior Y-sutural cataract and dental findings.

Keywords: Cataract; NHS; Nance–Horan; X-linked; infantile.

MeSH terms

  • Adult
  • Cataract / congenital*
  • Cataract / ethnology
  • Cataract / genetics
  • Cataract / metabolism
  • DNA / genetics*
  • DNA Mutational Analysis
  • Ethnicity*
  • Exons
  • Female
  • Genetic Diseases, X-Linked / ethnology
  • Genetic Diseases, X-Linked / genetics*
  • Genetic Diseases, X-Linked / metabolism
  • Humans
  • Male
  • Membrane Proteins
  • Mutation*
  • Nuclear Proteins / genetics*
  • Nuclear Proteins / metabolism
  • Pedigree
  • Phenotype
  • Polymerase Chain Reaction
  • Tooth Abnormalities / ethnology
  • Tooth Abnormalities / genetics*
  • Tooth Abnormalities / metabolism

Substances

  • Membrane Proteins
  • NHS protein, human
  • Nuclear Proteins
  • DNA

Supplementary concepts

  • Nance-Horan syndrome