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Hunter syndrome


Hunter syndrome, or mucopolysaccharidosis Type II, is a lysosomal storage disease caused by a deficient (or absent) enzyme, iduronate-2-sulfatase (I2S). :544 The syndrome is named after physician Charles A. Hunter (1873-1955), who first described it in 1917. Born in...
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Hunter syndrome — Comprehensive overview covers causes, treatment of this rare metabolic disorder. ... Hunter syndrome is a rare genetic disorder that occurs ...
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Hunter syndrome — Comprehensive overview covers causes, treatment of this rare metabolic disorder. ... Hunter syndrome is one type of a group of inherited ...
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Hunter syndrome ( ′həntər ′sin′drōm ) ( medicine ) An X-linked recessive disease in which a deficiency of the enzyme iduronate sulfatase leads to the
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Hunter syndrome — Comprehensive overview covers causes, treatment of this rare metabolic disorder. ... Hunter syndrome is a rare genetic disorder that ...
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Hunter syndrome is an inherited disease in which long chains of sugar molecules ... who want to have children and who have a family history of Hunter syndrome. ...
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Article describes Hunter syndrome (mucopolysaccharidosis II), its symptoms, diagnosis, and treatment. ... Hunter syndrome can occur in any ethnic group; a ...
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Important It is possible that the main title of the report Hunter Syndrome is not the name you expected. Please check the synonyms listing to find the alternate ...
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In Hunter syndrome, GAG build up in cells throughout the body due to a ... Physical manifestations for some people with Hunter syndrome ...
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Information on hunter syndrome, or mucopolysaccharidosis type 2, or MPS II. Learn about symptoms, ... Managing Hunter Syndrome. Community Voices. Newsletter ...
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ImportantIt is possible that the main title of the report Hunter Syndromeis not the name you expected. ... Hunter syndrome, also known as mucopolysaccharidosis ...
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Hunter's syndrome (Charles A. Hunter): Rare hereditary disorder characterised by dwarfism, a coarse facies, hepatosplenomegaly, digital contractures and mental ...
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Hunter syndrome, also known as mucopolysaccharidosis II, is a rare inborn error ... the main title of the report Hunter Syndrome is not the name you expected. ...
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Hunter syndrome is inherited as an X-linked recessive disease. ... The metabolic abnormality that causes Hunter syndrome is a lack of the enzyme ...
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Hunter syndrome is an inherited disease in which long chains of sugar molecules ... who want to have children and who have a family history of Hunter syndrome. ...
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Hunter syndrome is inherited as an X-linked recessive disease. ... The metabolic abnormality that causes Hunter syndrome is a lack of the enzyme ...
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Hunter syndrome is inherited as an X-linked recessive disease. ... The metabolic abnormality that causes Hunter syndrome is a lack of the enzyme ...
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h2g2 is the unconventional guide to life, the universe and everything, a guide that's written by visitors to the ... Hunter syndrome, or MPS-II is a rare ...
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Hunter syndrome - Overview, Hunter syndrome is a hereditary disease in which the ... Hunter syndrome is inherited as an X-linked recessive disease. ...
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