Fig. 1From: Neonatal cholestasis is an early liver manifestation of children with acid sphingomyelinase deficiencyA diagnostic algorithm for neonatal cholestasis. TPN, total parenteral nutrition; GGT, γ-glutamyl transpeptidase; TBA, total bile acids; ULN, upper limit of normal value; BASD, bile acid synthesis defect; PFIC, progressive familial intrahepatic cholestasis; ARCS, arthrogryposis, renal dysfunction, and cholestasis syndrome; TTE, transthoracic echocardiography; BM, bone marrow; ALGS, alagille syndrome; CF, cystic fibrosis; NP-C, Niemann-Pick disease type C; ASMD, acid sphingomyelinase deficiencyBack to article page