Sanfilippo disease in Greece

Clin Genet. 1986 Feb;29(2):129-32. doi: 10.1111/j.1399-0004.1986.tb01235.x.

Abstract

In a series of cases collected in most parts of the world, Sanfilippo disease type A is more frequent than type B. Skin biopsies were obtained from Greek patients suspected for Sanfilippo disease and cultured fibroblasts were assayed for both N-acetyl-a-glucosaminidase and sulfamidase activity. Eleven patients with Sanfilippo disease were identified. Ten of them were type B and one type A. The 10 patients with type B came from East-Central Greece and the neighboring areas of Thessaly and Macedonia. Both parents of the type A patient were from the Greek ethnic community of Turkey. It remains unknown whether or not the higher frequency of type B than type A appears only in Greece or if it occurs in other Mediterranean countries as well.

MeSH terms

  • Acetylglucosaminidase / deficiency
  • Cells, Cultured
  • Fibroblasts / enzymology
  • Greece
  • Humans
  • Hydrolases / deficiency
  • Mucopolysaccharidoses / epidemiology*
  • Mucopolysaccharidosis III / epidemiology*
  • Mucopolysaccharidosis III / genetics

Substances

  • Hydrolases
  • N-sulfoglucosamine sulfohydrolase
  • Acetylglucosaminidase