A Case Report of a Prenatally Missed Mowat-Wilson Syndrome With Isolated Corpus Callosum Agenesis

Mowat–Wilson syndrome (MWS) is an autosomal dominant genetic disorder caused by ZEB2 gene mutations, manifesting with unique facial characteristics, moderate to severe intellectual problems, and congenital malformations as Hirschsprung disease, genital and ophthalmological anomalies, and congenital...

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Detalles Bibliográficos
Autores principales: Şenbil, Nesrin, Arslan, Zeynep, Sayın Kocakap, Derya Beyza, Bilgili, Yasemin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2021
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8072816/
https://www.ncbi.nlm.nih.gov/pubmed/33997095
http://dx.doi.org/10.1177/2329048X211006511

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8072816/
https://www.ncbi.nlm.nih.gov/pubmed/33997095
http://dx.doi.org/10.1177/2329048X211006511

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