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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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Detalhes bibliográficos
Publicado no:Case Rep Genet
Main Authors: Bulut, Ozgul, Ince, Zeynep, Altunoglu, Umut, Yildirim, Sukran, Coban, Asuman
Formato: Artigo
Idioma:Inglês
Publicado em: Hindawi 2017
Assuntos:
Acesso em linha: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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