Biliary Atresia in an Infant Presenting With Kabuki Syndrome: An Autopsy Report and Review of the Literature-Reference-Cited by-同舟云学术

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

Published:2023-03-28 Issue:3 Volume:26 Page:318-320
ISSN:1093-5266
Container-title:Pediatric and Developmental Pathology
language:en
Short-container-title:Pediatr Dev Pathol

Author:

Tralongo Pietro¹,De Bartolo Debora²,Silvestri Nicola³,Mercuri Giulia³,Oliva Antonio³,Arena Vincenzo¹

Affiliation:

1. 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

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

3. Institute of Public Health, Section of Legal Medicine, Fondazione Policlinico A. Gemelli IRCCS, Universita Cattolica Del Sacro Cuore, Italy

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.

Publisher

SAGE Publications

Subject

General Medicine,Pathology and Forensic Medicine,Pediatrics, Perinatology and Child Health

Link

http://journals.sagepub.com/doi/pdf/10.1177/10935266231161384

Reference9 articles.

1. Biliary atresia

2. Current management of biliary atresia

3. Unexpected life-threatening complications in Kabuki syndrome

4. Biliary atresia in Kabuki syndrome

5. Biliary atresia and Kabuki syndrome: Another case with long-term follow-up

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