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...
| Váldodahkkit: | , , , , , |
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| Materiálatiipa: | Artihkal |
| Giella: | Russian |
| Almmustuhtton: |
Gastro LLC
2016-08-01
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| Ráidu: | Российский журнал гастроэнтерологии, гепатологии, колопроктологии |
| Fáttát: | |
| Liŋkkat: | https://www.gastro-j.ru/jour/article/view/59 |