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Schinzel-Giedion Syndrome with Congenital Megacalycosis in a Turkish Patient: Report of SETBP1 Mutation and Literature Review of the Clinical Features

Schinzel-Giedion syndrome (SGS) is a rare autosomal dominant disorder that results in facial dysmorphism, multiple congenital anomalies, and an increased risk of malignancy. Recently, using exome sequencing, de novo heterozygous mutations in the SETBP1 gene have been identified in patients with SGS....

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Enregistré dans:
Détails bibliographiques
Publié dans:Case Rep Genet
Auteurs principaux: Bulut, Ozgul, Ince, Zeynep, Altunoglu, Umut, Yildirim, Sukran, Coban, Asuman
Format: Artigo
Langue:Inglês
Publié: Hindawi 2017
Sujets:
Accès en ligne:https://ncbi.nlm.nih.gov/pmc/articles/PMC5733194/
https://ncbi.nlm.nih.gov/pubmed/29333303
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2017/3740524
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