Diagnosis in bile acid-CoA: amino acid N-acyltransferase deficiency

胆汁酸辅酶A的诊断:氨基酸N-酰基转移酶缺乏症

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作者:Nedim Hadžić, Laura N Bull, Peter T Clayton, A S Knisely

Abstract

Cholate-CoA ligase (CCL) and bile acid-CoA: amino acid N-acyltransferase (BAAT) sequentially mediate bile-acid amidation. Defects can cause intrahepatic cholestasis. Distinction has required gene sequencing. We assessed potential clinical utility of immunostaining of liver for CCL and BAAT. Using commercially available antibodies against BAAT and CCL, we immunostained liver from an infant with jaundice, deficiency of amidated bile acids, and transcription-terminating mutation in BAAT. CCL was normally expressed. BAAT expression was not detected. Immunostaining may facilitate diagnosis in bile-acid amidation defects.

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