| Hurler's disease |
Hurler's syndrome: hereditary disease (autosomal recessive) consisting of an error is mucopolysaccharide metabolism; characterized by severe abnormalities in development of skeletal cartilage and bone and mental retardation
출처: wordnet.princeton.edu/perl/webwn
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|---|---|
| Hurler's syndrome |
hereditary disease (autosomal recessive) consisting of an error is mucopolysaccharide metabolism; characterized by severe abnormalities in development of skeletal cartilage and bone and mental retardation
출처: wordnet.princeton.edu/perl/webwn
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| Hurler-Scheie syndrome |
Clinical spectrum that is intermediate between Hurler and Scheie syndromes. See MPS I
출처: www.mpssociety.org/lib-glossary.html
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| Hurler-Scheie s. |
one of the three allelic disorders of mucopolysaccharidosis I, with clinical features intermediate between the Hurler and the Scheie syndromes, caused by deficiency of L-iduronidase, and specifically characterized by receding chin (micrognathism). Symptoms include mental retardation, dwarfism, dysostosis multiplex, corneal clouding, deafness, hernia, stiff joints (claw hand), and valvular heart disease. Patients survive until their late teens or twenties. Called also mucopolysaccharidosis IH/S.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| Hurst d. |
acute necrotizing hemorrhagic encephalomyelitis.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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