婴儿期卡布奇诺综合征伴胆道闭锁：尸检报告及文献复习。

Biliary Atresia in an Infant Presenting With Kabuki Syndrome: An Autopsy Report and Review of the Literature.

机构信息

Area of Pathology, Department of Woman and Child Health and Public Health, Fondazione Policlinico Universitario A. Gemelli IRCCS, Istituto di Anatomia Patologica, Universita Cattolica Del Sacro Cuore, Rome, Italy.

Anatomia Patologica, Ospedale Santa Maria di Ca' Foncello, Treviso, Italy.

出版信息

Pediatr Dev Pathol. 2023 May-Jun;26(3):318-320. doi: 10.1177/10935266231161384. Epub 2023 Mar 28.

DOI:10.1177/10935266231161384

PMID:36974991

原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10291101/

Abstract

Biliary atresia (BA) is an inflammatory obliterative cholangiopathy which is very common during neonatal and infancy period. We present an autopsy report of a BA in an infant suffering from a genetic syndrome.

摘要

先天性胆道闭锁（BA）是一种新生儿和婴儿期常见的炎症性闭塞性胆管病。我们报告了一例患有遗传综合征的婴儿的 BA 尸检报告。