Hedgehog Signal Defect Leading to Familial Exudative Vitreoretinopathy-Like Disease and Gastrointestinal Malformation.

Sahinoglu Keskek, Nedime; Akkoyun, Imren; Temiz, Abdülkerim; Kütük, Özgür

Sahinoglu Keskek, Nedime; Akkoyun, Imren; Temiz, Abdülkerim; Kütük, Özgür.

Afiliación

Sahinoglu Keskek N; Baskent University Faculty of Medicine, Adana Research and Training Center, Department of Ophthalmology, Adana, Turkey.
Akkoyun I; Baskent University Faculty of Medicine, Department of Ophthalmology, Ankara, Turkey.
Temiz A; Baskent University Faculty of Medicine, Adana Research and Training Center, Department of Pediatric Surgery, Adana, Turkey.
Kütük Ö; Baskent University Faculty of Medicine, Adana Research and Training Center, Department of Medical Genetics, Adana, Turkey.

Turk J Ophthalmol ; 52(3): 174-178, 2022 06 29.

Article en En | MEDLINE | ID: mdl-35770050

Asunto(s)

Oftalmopatías; Enfermedades de la Retina; Enfermedades Vasculares; Vitreorretinopatías Exudativas Familiares; Proteínas Hedgehog/genética; Humanos; Lactante; Recién Nacido; Enfermedades de la Retina/diagnóstico

Palabras clave

Familial exudative vitreoretinopathy; gastrointestinal tract malformations; genetic; hedgehog pathway; retinal vasculardisease

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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Enfermedades de la Retina / Enfermedades Vasculares / Oftalmopatías Tipo de estudio: Diagnostic_studies Límite: Humans / Infant / Newborn Idioma: En Revista: Turk J Ophthalmol Año: 2022 Tipo del documento: Article País de afiliación: Turquía Pais de publicación: Turquía

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