Mucopolysaccharidoses - Get information and read articles on Mucopolysaccharidoses signs, symptoms, causes, treatment, prevention and diagnosis at onlymyhealth.com, your complete health guide.
The mucopolysaccharidoses are a group of inherited metabolic diseases caused by the absence or malfunctioning of certain enzymes needed to break down molecules
Mucopolysaccharidoses is a group of inherited metabolic diseases. Diagnosis of Mucopolysaccharidoses often can be made through clinical examination and urine tests.
Physical symptoms of Mucopolysaccharidoses include coarse or rough facial features, short stature with disproportionately short trunk, and other skeletal irregularities, thickened skin, hernias, and excessive body hair growth.
Mucopolysaccharidoses: When both people in a couple have the defective gene, each pregnancy carries with it a one in four chance that the child will be affected.
Seven distinct clinical types and numerous subtypes of the mucopolysaccharidoses have been identified.
Treatment of Mucopolysaccharidoses: Medical care is directed at treating systemic conditions and improving the person's quality of life.