Clinical and molecular description of two cases of neonatal diabetes secondary to mutations in PDX1

Clinical and molecular description of two cases of neonatal diabetes secondary to mutations in PDX1

Pancreatic dysgenesis (PD) is a rare congenital disease, with less than 100 cases reported in the literature. In most cases, patients are asymptomatic and the diagnosis is made incidentally. In this report, we present the case of two brothers with a history of intrauterine growth retardation, low bi...

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Bibliographic Details
Main Authors: Nicolas Forero-Castro, Luis Carlos Ramirez, Juan Carlos Celis, Fernando Arturo Silva Henao, Fernando Leal Valencia
Format: Article
Language:English
Published: Bioscientifica 2023-07-01
Series:Endocrinology, Diabetes & Metabolism Case Reports
Online Access:https://edm.bioscientifica.com/view/journals/edm/2023/3/EDM22-0383.xml

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