Case report: ZFYVE19 gene mutation is associated with familial cholestasis
The etiology of cholestatic liver disease is complex, with clinical manifestations being nonspecific, and biochemical abnormalities mainly characterized by elevated alkaline phosphatase (ALP) and glutamyl transpeptidase (GGT).Due to the lack of specific symptoms Drain Cap and diverse causes, the diagnosis poses certain challenges.Here, we present a