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.

Afiliação

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 em En | MEDLINE | ID: mdl-35770050

Assuntos

Oftalmopatias; Doenças Retinianas; Doenças Vasculares; Vitreorretinopatias Exsudativas Familiares; Proteínas Hedgehog/genética; Humanos; Lactente; Recém-Nascido; Doenças Retinianas/diagnóstico

Palavras-chave

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

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doenças Retinianas / Doenças Vasculares / Oftalmopatias Tipo de estudo: Diagnostic_studies Limite: Humans / Infant / Newborn Idioma: En Revista: Turk J Ophthalmol Ano de publicação: 2022 Tipo de documento: Article

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