Genetic heterogeneity and clinical variability in the Sanfilippo syndrome (types A, B, and C)

Clin Genet. 1981 Aug;20(2):152-60. doi: 10.1111/j.1399-0004.1981.tb01821.x.

Abstract

A study of 73 patients with the Sanfilippo syndrome (36 patients with Sanfilippo A disease, 23 with Sanfilippo B disease and 14 with Sanfilippo C disease) revealed both intertype and intratype variability. The course of the disease was relatively mild in Sanfilippo B disease and dementia was less severe. Type A showed earlier onset with more severe clinical manifestations and an earlier age at death. Sanfilippo C disease was slightly less severe than Sanfilippo A disease. The intratype variability may be explained in part by differences in genetic and environmental background. In Sanfilippo B disease, genetic heterogeneity is suggested by the observation of a more severe and a mild variant, and this variation may be due to the involvement of different allelic mutations. The intrafamilial variability of the different types was small, but in three families with Sanfilippo B disease intrafamilial variability was evident.

MeSH terms

  • Adolescent
  • Adult
  • Child
  • Child, Preschool
  • Dementia / genetics
  • Female
  • Genetic Variation*
  • Humans
  • Infant
  • Male
  • Mucopolysaccharidoses / genetics*
  • Mucopolysaccharidosis III / classification
  • Mucopolysaccharidosis III / genetics*
  • Mucopolysaccharidosis III / mortality