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Rare forms of nonalcoholic fatty liver disease: hereditary lysosomal acid lipase deficiency

Aim of review. To acquaint general practitioners with a rarely diagnosed disease - the hereditary deficiency of lysosomal acid lipase (DLAL) which can develop under the «mask» non-alcoholic fatty liver disease (NAFLD). Summary. There are two forms of DLAL clinical manifestations: as fulminant lethal...

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Autori principali: M. V. Mayevskaya, V. T. Ivashkin, M. S. Zharkova, T. P. Nekrasova, G. I. Ayusheva, R. V. Maslennikov
Natura: Artigo
Lingua:Russo
Pubblicazione: Gastro LLC 2016-08-01
Serie:Российский журнал гастроэнтерологии, гепатологии, колопроктологии
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Accesso online:https://www.gastro-j.ru/jour/article/view/59
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