Maturity‐onset diabetes of the young: Different diabetes in an infant with cystic fibrosis

Cystic fibrosis (CF) is one of the most common autosomal recessive and multisystemic diseases. CF affects many systems. One of these systems is the endocrine and exocrine functions of the pancreas, causing cystic fibrosis‐related diabetes, which is extremely complex and has unique pathogenesis. Matu...

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Veröffentlicht in:Pediatric pulmonology 2020-05, Vol.55 (5), p.E5-E7
Hauptverfasser: Hangül, Melih, Erdoğan, Murat, Hatipoğlu, Nihal, Köse, Mehmet
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container_issue 5
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container_title Pediatric pulmonology
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creator Hangül, Melih
Erdoğan, Murat
Hatipoğlu, Nihal
Köse, Mehmet
description Cystic fibrosis (CF) is one of the most common autosomal recessive and multisystemic diseases. CF affects many systems. One of these systems is the endocrine and exocrine functions of the pancreas, causing cystic fibrosis‐related diabetes, which is extremely complex and has unique pathogenesis. Maturity‐onset diabetes of the young (MODY) is a rare type of diabetes with autosomal dominant inheritance and is not expected in patients with CF. In this study, we present MODY due to a novel glucokinase gene mutation, which is an unexpected form of diabetes in patients with CF. This is previously unreported in the literature.
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subjects Cystic fibrosis
Diabetes
maturity‐onset diabetes of the young
novel GCK gene mutation
title Maturity‐onset diabetes of the young: Different diabetes in an infant with cystic fibrosis
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