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Congenital etiologies of exocrine pancreatic insufficiency

Congenital exocrine pancreatic insufficiency is a rare condition. In a vast majority of patients, exocrine dysfunction occurs as part of a multisystemic disease, the most prevalent being cystic fibrosis and Shwachman-Bodian-Diamond syndrome. Recent fundamental studies have increased our understandin...

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Autores principales: Scheers, Isabelle, Berardis, Silvia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9354839/
https://www.ncbi.nlm.nih.gov/pubmed/35935370
http://dx.doi.org/10.3389/fped.2022.909925
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author Scheers, Isabelle
Berardis, Silvia
author_facet Scheers, Isabelle
Berardis, Silvia
author_sort Scheers, Isabelle
collection PubMed
description Congenital exocrine pancreatic insufficiency is a rare condition. In a vast majority of patients, exocrine dysfunction occurs as part of a multisystemic disease, the most prevalent being cystic fibrosis and Shwachman-Bodian-Diamond syndrome. Recent fundamental studies have increased our understanding of the pathophysiology of these diseases. Exocrine pancreatic dysfunction should be considered in children with failure to thrive and fatty stools. Treatment is mainly supportive and consists of pancreatic enzyme replacement and liposoluble vitamins supplementation.
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spelling pubmed-93548392022-08-06 Congenital etiologies of exocrine pancreatic insufficiency Scheers, Isabelle Berardis, Silvia Front Pediatr Pediatrics Congenital exocrine pancreatic insufficiency is a rare condition. In a vast majority of patients, exocrine dysfunction occurs as part of a multisystemic disease, the most prevalent being cystic fibrosis and Shwachman-Bodian-Diamond syndrome. Recent fundamental studies have increased our understanding of the pathophysiology of these diseases. Exocrine pancreatic dysfunction should be considered in children with failure to thrive and fatty stools. Treatment is mainly supportive and consists of pancreatic enzyme replacement and liposoluble vitamins supplementation. Frontiers Media S.A. 2022-07-22 /pmc/articles/PMC9354839/ /pubmed/35935370 http://dx.doi.org/10.3389/fped.2022.909925 Text en Copyright © 2022 Scheers and Berardis. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Pediatrics
Scheers, Isabelle
Berardis, Silvia
Congenital etiologies of exocrine pancreatic insufficiency
title Congenital etiologies of exocrine pancreatic insufficiency
title_full Congenital etiologies of exocrine pancreatic insufficiency
title_fullStr Congenital etiologies of exocrine pancreatic insufficiency
title_full_unstemmed Congenital etiologies of exocrine pancreatic insufficiency
title_short Congenital etiologies of exocrine pancreatic insufficiency
title_sort congenital etiologies of exocrine pancreatic insufficiency
topic Pediatrics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9354839/
https://www.ncbi.nlm.nih.gov/pubmed/35935370
http://dx.doi.org/10.3389/fped.2022.909925
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