Case Report: Neonatal Diabetes Mellitus Caused by a Novel GLIS3 Mutation in Twins

BACKGROUND: Mutations in GLIS3 cause a rare syndrome characterized by neonatal diabetes mellitus (NDM), congenital hypothyroidism, congenital glaucoma and cystic kidneys. To date, 14 mutations in GLIS3 have been reported, inherited in an autosomal recessive manner. GLIS3 is a key transcription facto...

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Bibliografiske detaljer
Udgivet i:Front Endocrinol (Lausanne)
Main Authors: London, Shira, De Franco, Elisa, Elias-Assad, Ghadir, Barhoum, Marie Noufi, Felszer, Clari, Paniakov, Marina, Weiner, Scott A., Tenenbaum-Rakover, Yardena
Format: Artigo
Sprog:Inglês
Udgivet: Frontiers Media S.A. 2021
Fag:
Endocrinology
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC8169976/
https://ncbi.nlm.nih.gov/pubmed/34093443
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fendo.2021.673755
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