A Possible Incomplete Form of Treacher Collins Syndrome: A Case Report

Treacher Collins syndrome (TCS) is a rare genetic disorder that affects craniofacial development due to malformation of the first and second branchial arches. The TCOF1 gene is mainly responsible for this condition. Here, we present a case of a 13-year-old adolescent girl with complaints of maligned...

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Detalles Bibliográficos
Autores principales: Tarang, Tanmay, Vagha, Keta, Kiran, Adithya, Singh, Kushagra
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2022
Materias:
Pediatrics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9650923/
https://www.ncbi.nlm.nih.gov/pubmed/36381924
http://dx.doi.org/10.7759/cureus.30203

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9650923/
https://www.ncbi.nlm.nih.gov/pubmed/36381924
http://dx.doi.org/10.7759/cureus.30203

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