Monogenic Defects of Beta Cell Function: From Clinical Suspicion to Genetic Diagnosis and Management of Rare Types of Diabetes.
MODY
mitochondrial diabetes
monogenic diabetes
neonatal diabetes
syndromic diabetes
Journal
International journal of molecular sciences
ISSN: 1422-0067
Titre abrégé: Int J Mol Sci
Pays: Switzerland
ID NLM: 101092791
Informations de publication
Date de publication:
29 Sep 2024
29 Sep 2024
Historique:
received:
26
08
2024
revised:
25
09
2024
accepted:
27
09
2024
medline:
16
10
2024
pubmed:
16
10
2024
entrez:
16
10
2024
Statut:
epublish
Résumé
Monogenic defects of beta cell function refer to a group of rare disorders that are characterized by early-onset diabetes mellitus due to a single gene mutation affecting insulin secretion. It accounts for up to 5% of all pediatric diabetes cases and includes transient or permanent neonatal diabetes, maturity-onset diabetes of the young (MODY), and various syndromes associated with diabetes. Causative mutations have been identified in genes regulating the development or function of the pancreatic beta cells responsible for normal insulin production and/or release. To date, more than 40 monogenic diabetes subtypes have been described, with those caused by mutations in
Identifiants
pubmed: 39408828
pii: ijms251910501
doi: 10.3390/ijms251910501
pii:
doi:
Substances chimiques
Hepatocyte Nuclear Factor 1-alpha
0
HNF1A protein, human
0
Types de publication
Journal Article
Review
Langues
eng
Sous-ensembles de citation
IM