Inherited metabolic
liver disease has complex etiologies and various types, and its clinical manifestations lack
specificity, which may
lead to
missed diagnosis and
misdiagnosis. A
clinical diagnosis should be given based on symptoms, signs,
laboratory examination, imaging findings,
liver biopsy, and
gene detection, in order to provide a basis for early
treatment. Therefore, clues from clinical examination
play an important
role in the
diagnosis of this
disease. This article summarizes the clinical clues and diagnostic ideas of inherited metabolic
liver disease.