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...
Main Authors: | , , , , |
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Format: | Article |
Language: | English |
Published: |
Bioscientifica
2023-07-01
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Series: | Endocrinology, Diabetes & Metabolism Case Reports |
Online Access: | https://edm.bioscientifica.com/view/journals/edm/2023/3/EDM22-0383.xml |