Hunter syndrome

Hunter syndrome
Recessive mucopolysaccharidosis, X-linked, in which dermatan and heparan sulphates are not degraded. Because two lysosomal enzymes (heparan sulphate sulphatase and a -iduronidase) are involved in the breakdown of these glycosaminoglycans, fibroblasts from Hunter\'s syndrome will complement the fibroblasts from Hurler\'s patients in culture; by recapture of lysosomal enzymes from the medium, both types of cells in mixed culture become competent to digest glycosaminoglycans.

Dictionary of molecular biology. 2004.

Look at other dictionaries:

  • Hunter syndrome — Classification and external resources ICD 10 E76.1 ICD 9 277.5 …   Wikipedia

  • Hunter syndrome — A genetic metabolic disorder that arises from deficiency of the enzyme iduronate sulfatase, resulting in tissue deposits of molecules called mucopolysaccharides. The characteristic features of Hunter syndrome include dwarfism, bone deformities, a …   Medical dictionary

  • Hunter's syndrome — or Hunter syndrome hən tər(z) n a mucopolysaccharidosis that is similar to Hurler s syndrome but is inherited as a sex linked recessive trait and has milder symptoms Hunter Charles (1873 1955) Canadian physician. Hunter published his original… …   Medical dictionary

  • Hunter (disambiguation) — A hunter is someone who engages in the act of hunting.Hunter may also refer to:People* Hunter (name), a given name and a family name (including a list of people with that name)PlacesAustralia* Division of Hunter, electoral district in the… …   Wikipedia

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  • syndrome — The aggregate of symptoms and signs associated with any morbid process, and constituting together the picture of the disease. SEE ALSO: disease. [G. s., a running together, tumultuous concourse; (in med.) a concurrence of symptoms, fr. syn,… …   Medical dictionary

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