Inborn errors of metabolism in the differential diagnosis of fatty liver disease

被引:12
|
作者
Yildiz, Yilmaz [1 ]
Sivri, Hatice Serap [2 ]
机构
[1] Dr Sami Ulus Training & Res Hosp Matern & Childre, Pediat Metab Dis Unit, Ankara, Turkey
[2] Hacettepe Univ, Sch Med, Dept Pediat, Div Metab Dis, Ankara, Turkey
来源
TURKISH JOURNAL OF GASTROENTEROLOGY | 2020年 / 31卷 / 01期
关键词
Inborn errors of metabolism; liver steatosis; metabolic diseases; nonalcoholic fatty liver disease; steatohepatitis; GLYCOGEN-STORAGE-DISEASE; ACID OXIDATION DISORDERS; PHENOTYPIC SPECTRUM; DEFICIENCY; FEATURES; FAILURE; HYPOBETALIPOPROTEINEMIA; IDENTIFICATION; CHOLESTEROL; INVOLVEMENT;
D O I
10.5152/tjg.2019.19367
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Nonalcoholic fatty liver disease (NAFLD) has become the most common chronic liver disease across all age groups. Obesity, diabetes, and metabolic syndrome, are the primary causes that are closely linked with the development of NAFLD. However, in young children, rare inborn errors of metabolism are predominant secondary causes of NAFLD. Furthermore, inborn errors of metabolism causing hepatosteatosis are often misdiagnosed as NAFLD in adolescents and adults. Many inborn errors of metabolism are treatable disorders and therefore require special consideration. This review aims to summarize the basic characteristics and diagnostic clues of inborn errors of metabolism associated with fatty liver disease. A suggested clinical and laboratory diagnostic approach is also discussed.
引用
收藏
页码:3 / 16
页数:14
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