Clinical variability and genetic heterogeneity within the Acadian Usher population

Am J Med Genet. 1992 Aug 1;43(6):964-9. doi: 10.1002/ajmg.1320430612.

Abstract

A number of Usher syndrome (USH) families are found among the French-Acadians living in southwestern Louisiana. These families are descended from a few common ancestors, suggesting that USH may be homogeneous within this ethnic group. However, we report distinct phenotypic variability. Based on differences in psychomotor development and tests of auditory and vestibular function, Acadian individuals with both USH Type 1 and Type 2 can be identified. One additional family, with unusual findings, represents a third clinical phenotype. Linkage data strongly support these clinical observations.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Blindness / genetics*
  • Chromosomes, Human, Pair 1
  • Ethnicity
  • Female
  • Genetic Markers
  • Hearing Disorders / classification
  • Hearing Disorders / genetics*
  • Humans
  • Louisiana
  • Male
  • Pedigree
  • Phenotype
  • Syndrome

Substances

  • Genetic Markers