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Wolman's disease : ウィキペディア英語版 | Wolman disease
Wolman disease (also known as Wolman’s disease or early onset lysosomal acid lipase deficiency) is a rare genetic disorder caused by a deficiency of an enzyme known as lysosomal acid lipase (LAL or LIPA). This enzyme is necessary to break down certain lipids inside the cells. Deficiency of the LAL/LIPA enzyme causes a build-up of fat in the liver, gut and other parts of the body. * 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「Wolman disease」の詳細全文を読む
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