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单词 PDHC Deficiency Diseases
释义

PDHC Deficiency Diseases

《英文msh词典》PDHC Deficiency Diseases
[入口词] PDHC Deficiency Diseases
[主题词] Pyruvate Dehydrogenase Complex Deficiency Disease
[英文释义] An inherited metabolic disorder caused by deficient enzyme activity in the PYRUVATE DEHYDROGENASE COMPLEX,resulting in deficiency of acetyl CoA and reduced synthesis of acetylcholine. Two clinical forms are recognized: neonatal and juvenile. The neonatal form is a relatively common cause of lactic acidosis in the first weeks of life and may also feature an erythematous rash. The juvenile form presents with lactic acidosis,alopecia,intermittent ATAXIA,SEIZURES,and an erythematous rash. (From J Inherit Metab Dis 1996;19(4):452-62) Autosomal recessive and X-linked forms are caused by mutations in the genes for the three different enzyme components of this multisubunit pyruvate dehydrogenase complex. One of the mutations at Xp22.2-p22.1 in the gene for the E1 alpha component of the complex leads to LEIGH DISEASE.
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更新时间：2026/9/10 15:24:10