Treacher Collins syndrome: A case report and review of literature

Treacher Collins syndrome (TCS) is one of the rare genetic syndromes which is specified by symmetrical craniofacial dysmorphism without growth abnormalities or neurological disorders. The inheritance is usually autosomal dominant but sometimes it is a sporadic mutation. Prenatal diagnosis could be r...

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Detalles Bibliográficos
Autores principales: Kolsi, Nadia, Boudaya, Fatma, Ben Thabet, Afef, Charfi, Manel, Regaieg, Chiraz, Bouraoui, Amira, Regaieg, Ridha, Hentati, Nedia, Hamed, Amel Ben, Gargouri, Abdellatif
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9794916/
https://www.ncbi.nlm.nih.gov/pubmed/36590667
http://dx.doi.org/10.1002/ccr3.6782

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9794916/
https://www.ncbi.nlm.nih.gov/pubmed/36590667
http://dx.doi.org/10.1002/ccr3.6782

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