Wolcott-Rallison syndrome: a case series of three patients

Neonatal diabetes is a rare disease with incidence estimated at 1 in 300,000 to 1 in 400,000 live births. Walcott-Rallison syndrome has been identified as the most common cause of permanent neonatal diabetes in consanguineous families caused by mutations in eukaryotic translation initiation factor 2...

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Veröffentlicht in:	Pediatric endocrinology, diabetes, and metabolism diabetes, and metabolism, 2022, Vol.28 (3), p.238-240
Hauptverfasser:	Memon, Fozia, Arif, Muzna, Kirmani, Salman, Humayun, Khadija
Format:	Artikel
Sprache:	eng
Schlagworte:	Case report | Opis przypadku Diabetes Mellitus - etiology Diabetes Mellitus, Type 1 - complications Diabetes Mellitus, Type 1 - diagnosis Diabetes Mellitus, Type 1 - genetics Epiphyses - abnormalities Glucose Humans Insulins Mutation Osteochondrodysplasias - complications Osteochondrodysplasias - diagnosis Osteochondrodysplasias - genetics Prokaryotic Initiation Factor-2 - genetics
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