The articles on this page are related to the series Irish folk group Clannad. For the category on the visual novel, please see :Category:Clannad (visual novel). ...
Found on
http://en.wikipedia.org/wiki/Hurler-Scheie_Syndrome
Hurler–Scheie syndrome (also known as `Mucopolysaccharidosis type I H-S`) is a cutaneous condition, also characterized by mild mental retardation and corneal clouding. == See also == ...
Found on
http://en.wikipedia.org/wiki/Hurler–Scheie_syndrome
(from the article `Scheie`s syndrome`) ...Hurler`s disease. Both syndromes are caused by a recessively inherited defect in the enzyme alpha-L-iduronidase, which is important in the ...
Found on
http://www.britannica.com/eb/a-z/h/85
<syndrome> Although clinically distinct diseases, fibroblasts from patients with Hurler syndrome and with Scheie syndrome do not cross complement in culture, suggesting that the enzyme defect is the same. ... (18 Nov 1997) ...
Found on
http://www.encyclo.co.uk/local/20973
(hur´lәr sha´) 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, ...
Found on
http://www.encyclo.co.uk/local/21001
Although clinically distinct diseases, fibroblasts from patients with Hurler's and with Scheie syndrome do not cross-complement in culture, suggesting that the enzyme defect is the same.
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http://www.encyclo.co.uk/visitor-contributions.php
Type: Term Pronunciation: hŭr′ler shā Definitions: 1. a phenotypic intermediate between Hurler syndrome and Scheie syndrome; a deficiency of α-l-iduronidase. Synonyms: type I H/S mucopolysaccharidosis
Found on
http://www.medilexicon.com/medicaldictionary.php?t=88103
No exact match found.
