Neonatal diabetes due to homozygous INS gene promoter mutations: Highly variable phenotype, remission and early relapse during the first 3 years of life.

Demiral, Meliha; Demirbilek, Huseyin; Çelik, Kiymet; Okur, Nilufer; Hussain, Khalid; Ozbek, Mehmet Nuri

Demiral, Meliha; Demirbilek, Huseyin; Çelik, Kiymet; Okur, Nilufer; Hussain, Khalid; Ozbek, Mehmet Nuri.

Afiliación

Demiral M; Gazi Yasargil Research and Training Hospital, Pediatric Endocrinology, Diyarbakir, Turkey.
Demirbilek H; Hacettepe University Faculty of Medicine, Department of Pediatric Endocrinology, Ankara, Turkey.
Çelik K; Gazi Yasargil Research and Training Hospital, Neonatology, Diyarbakir, Turkey.
Okur N; Gazi Yasargil Research and Training Hospital, Neonatology, Diyarbakir, Turkey.
Hussain K; Department of Pediatrics, Division of Endocrinology, Sidra Medicine, Doha, Qatar.
Ozbek MN; Gazi Yasargil Research and Training Hospital, Pediatric Endocrinology, Diyarbakir, Turkey.

Pediatr Diabetes ; 21(7): 1169-1175, 2020 11.

Article en En | MEDLINE | ID: mdl-32656923

Asunto(s)

Diabetes Mellitus/genética; Insulina/genética; Mutación/genética; Regiones Promotoras Genéticas/genética; Femenino; Humanos; Recién Nacido; Linaje; Fenotipo; Recurrencia; Remisión Espontánea

Palabras clave

INS gene; neonatal diabetes; permanent; relapse; transient

Texto completo

Imprimir

XML

PubMed Links

Buscar en Google

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Regiones Promotoras Genéticas / Diabetes Mellitus / Insulina / Mutación Límite: Female / Humans / Newborn Idioma: En Revista: Pediatr Diabetes Asunto de la revista: ENDOCRINOLOGIA Año: 2020 Tipo del documento: Article País de afiliación: Turquía

Texto completo

Imprimir

XML

PubMed Links

Buscar en Google