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...
| Hlavní autoři: | , , , , , |
|---|---|
| Médium: | Článek |
| Jazyk: | Russian |
| Vydáno: |
Gastro LLC
2016-08-01
|
| Edice: | Российский журнал гастроэнтерологии, гепатологии, колопроктологии |
| Témata: | |
| On-line přístup: | https://www.gastro-j.ru/jour/article/view/59 |