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Transient neonatal diabetes mellitus and activating mutation in the KCNJ11 gene in two siblings.
Kamoun, T; Chabchoub, I; Ben Ameur, S; Kmiha, S; Aloulou, H; Cave, H; Polak, M; Hachicha, M.
Afiliación
  • Kamoun T; Faculty of medicine Sfax, university of Sfax, Sfax, Tunisia; Service de pédiatrie, pediatric department, Hédi Chaker hospital, El Ain street K 0.5, 3029 Sfax, Tunisia.
  • Chabchoub I; Faculty of medicine Sfax, university of Sfax, Sfax, Tunisia; Service de pédiatrie, pediatric department, Hédi Chaker hospital, El Ain street K 0.5, 3029 Sfax, Tunisia.
  • Ben Ameur S; Faculty of medicine Sfax, university of Sfax, Sfax, Tunisia; Service de pédiatrie, pediatric department, Hédi Chaker hospital, El Ain street K 0.5, 3029 Sfax, Tunisia. Electronic address: benameursalma@gmail.com.
  • Kmiha S; Faculty of medicine Sfax, university of Sfax, Sfax, Tunisia; Service de pédiatrie, pediatric department, Hédi Chaker hospital, El Ain street K 0.5, 3029 Sfax, Tunisia.
  • Aloulou H; Faculty of medicine Sfax, university of Sfax, Sfax, Tunisia; Service de pédiatrie, pediatric department, Hédi Chaker hospital, El Ain street K 0.5, 3029 Sfax, Tunisia.
  • Cave H; Department of genetics, Robert-Debré university hospital, Assistance publique-Hôpitaux de Paris, 75019 Paris, France.
  • Polak M; Paediatric endocrine unit, centre of rare endocrine diseases of growth, Necker-Enfants-Malades hospital, AP-HP, 75012 Paris, France.
  • Hachicha M; Faculty of medicine Sfax, university of Sfax, Sfax, Tunisia; Service de pédiatrie, pediatric department, Hédi Chaker hospital, El Ain street K 0.5, 3029 Sfax, Tunisia.
Arch Pediatr ; 24(5): 453-456, 2017 May.
Article en En | MEDLINE | ID: mdl-28347637

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Cromosomas Humanos Par 6 / Canales de Potasio de Rectificación Interna / Diabetes Mellitus / Tamización de Portadores Genéticos / Enfermedades del Recién Nacido Tipo de estudio: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adolescent / Child / Child, preschool / Humans / Infant / Male / Newborn Idioma: En Año: 2017 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Cromosomas Humanos Par 6 / Canales de Potasio de Rectificación Interna / Diabetes Mellitus / Tamización de Portadores Genéticos / Enfermedades del Recién Nacido Tipo de estudio: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adolescent / Child / Child, preschool / Humans / Infant / Male / Newborn Idioma: En Año: 2017 Tipo del documento: Article