A Large Turkish Cohort of Williams Syndrome: The Evaluation of Facial, Cardiovascular, and Neuropsychiatric Features

OBJECTIVE: Williams syndrome is caused by a microdeletion at 7q11.23 and is characterized by a distinctive face, cardiovascular disease, and intellectual disability with a specific cognitive and behavioral profile. This study aims to evaluate the clinical features and obtain important information th...

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Detalles Bibliográficos
Autores principales: Bozlak, Serdar, Uludağ Alkaya, Dilek, Kasap, Büşra, Yüksel Ülker, Aylin, Yıldız, Ceren Ayça, Altındağ, Veysel, Ülkersoy, İpek, Çifçi Sunamak, Evrim, Dedeoğlu, Reyhan, Tüysüz, Beyhan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Turkish Pediatrics Association 2023
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10081020/
https://www.ncbi.nlm.nih.gov/pubmed/36856356
http://dx.doi.org/10.5152/TurkArchPediatr.2023.22212

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10081020/
https://www.ncbi.nlm.nih.gov/pubmed/36856356
http://dx.doi.org/10.5152/TurkArchPediatr.2023.22212

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