Hurler syndrome, also known as mucopolysaccharidosis type I (MPS I), Hurler's
disease, also ... Genetic counseling can help parents who have a family history of
the mucopolysaccharidoses determi...
The historical term for the most severe version of the disease is “Hurler disease”
or "Hurler syndrome,” named after the doctor who first described this condition.
Home · Professional Reference; Hurler's Syndrome. Hurler's Syndrome .... Beck
M, Arn P, Giugliani R, et al; The natural history of MPS I: global perspectives from
MPS I has also been called Hurler, Hurler-Scheie and Scheie syndrome . Hurler
takes its name from Gertrude Hurler, the doctor who described a boy and girl ...
May 7, 2013 ... Hurler syndrome is a rare, inherited disease of metabolism in which a ... with a
family history of Hurler syndrome who are considering having ...
In Hurler syndrome, the body is missing an enzyme that breaks down large
molecules called glycosaminoglycans (GAG). As GAG molecules build up in the
607014 - HURLER SYNDROME - MUCOPOLYSACCHARIDOSIS TYPE IH; ...
Inheritance. Molecular Genetics. Population Genetics. Animal Model. History.
Hurler syndrome is the most severe form of mucopolysaccharidosis type 1 (MPS1
; see ... and testing should be offered to couples with a positive family history.
Hurler syndrome is a rare, inherited disorder in which a hereditary factor, or gene,
.... Amniocentesis: When there is a family history of any of the three MPH I ...
Mar 27, 2014 ... Results: Natural history data were available for 987 patients. ... Hurler syndrome,
the most severe form of MPS I, typically involves significant ...