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Genetic variations in patient with Parry–Romberg syndrome

Parry–Romberg syndrome is a rare craniofacial disorder which is characterized by progressive facial atrophy. The etiology and pathogenesis of the disease are not known. Herein, we report the genetic variants in patient with this disease. A 25-year-old woman was diagnosed with Parry–Romberg syndrome...

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Detalles Bibliográficos
Autores principales: Yu, Bao-Fu, Dong, Li-Ping, Dai, Chuan-Chang, Wei, Jiao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9829853/
https://www.ncbi.nlm.nih.gov/pubmed/36624141
http://dx.doi.org/10.1038/s41598-023-27597-1