Wolman disease

名词 n.
中文释义

英文释义

名词 n.
  1. A rare genetic disorder caused by deficiency of an enzyme known as lysosomal acid lipase (LAL or LIPA), necessary to break down certain lipids. uncountable

词源

Named after Moshe Wolman, one of the authors of the first case study, published in 1956.
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