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Kaufman oculocerebrofacial syndrome : ウィキペディア英語版 | Kaufman oculocerebrofacial syndrome
Kaufman oculocerebrofacial syndrome is an autosomal recessive congenital disorder characterized by mental retardation, microbrachycephaly, long narrow face, upslanting palpebral fissures, eye abnormalities, highly arched palate, preauricular skin tags and small mandible. It was characterized in 1971. Eight cases had been identified as of 1995. ==Genetics==
It appears to be due to a mutation in the E3 ubiquitin protein ligase (UBE3B). 〔Flex E, Ciolfi A, Caputo V, Fodale V, Leoni C, Melis D, Bedeschi MF, Mazzanti L, Pizzuti A, Tartaglia M, Zampino G (2013) Loss of function of the E3 ubiquitin-protein ligase UBE3B causes Kaufman oculocerebrofacial syndrome. J Med Genet 〕
抄文引用元・出典: フリー百科事典『 ウィキペディア(Wikipedia)』 ■ウィキペディアで「Kaufman oculocerebrofacial syndrome」の詳細全文を読む
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