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

被引:0
|
作者
Nedim Hadzi [1 ]
Laura N Bull [2 ]
Peter T Clayton [3 ]
AS Knisely [4 ]
机构
[1] Paediatric Liver Service and Institute of Liver Studies,King's College Hospital,London SE5 9RS,United Kingdom
[2] Liver Center Laboratory,University of California San Francisco,San Francisco,CA 94110,United States
[3] Biochemistry Research Group,Clinical and Molecular Genetics Unit,University College London Institute of Child Health,London WC1 N1EH,United Kingdom
[4] Institute of Liver Studies,King's College Hospital,London SE5 9RS,United Kingdom
基金
美国国家卫生研究院;
关键词
Amidation; Bile acid-CoA; Amino acid N-ac-yltransferase; Cholate-CoA ligase; Cholestasis; Conjugation; Electrospray ionisation-mass spectroscopy; Immunohistochemistry; Liver; Neonatal hepatitis; SLC27A5; Transmission electron microscopy;
D O I
暂无
中图分类号
R589 [代谢病];
学科分类号
1002 ; 100201 ;
摘要
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 bileacid amidation defects.
引用
收藏
页码:3322 / 3326
页数:5
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