MNX1 mutations causing neonatal diabetes: Review of the literature and report of a case with extra‐pancreatic congenital defects presenting in severe diabetic ketoacidosis

The MNX1 gene encodes a homeobox transcription factor found to be important for pancreatic beta cell differentiation and development. Mutations of the MNX1 gene that cause permanent neonatal diabetes mellitus (PNDM) are rare and have been reported in only two cases. Both cases presented with hypergl...

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Detalles Bibliográficos
Autores principales: Aly, Hanan Hassan, De Franco, Elisa, Flanagan, Sarah E., Elhenawy, Yasmine I.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Mini Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10034954/
https://www.ncbi.nlm.nih.gov/pubmed/36586106
http://dx.doi.org/10.1111/jdi.13968

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10034954/
https://www.ncbi.nlm.nih.gov/pubmed/36586106
http://dx.doi.org/10.1111/jdi.13968

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