Novel Compound Heterozygous Mutations in CTSC Gene in a Chinese Family with Papillon-Lefevre Syndrome

Papillon-Lefevre syndrome (PLS) (OMIM: 245000) is a rare autosomal recessive disorder characterized by palmoplantar hyperkeratosis and early onset periodontitis, resulting in the premature loss of the deciduous and permanent teeth. PLS is caused by mutations in the cathepsin C (CTSC) gene (OMIM: 602...

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Detalles Bibliográficos
Autores principales: Wang, Yuan, Zhang, Hanmei, Feng, Suying
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Dermatological Association; The Korean Society for Investigative Dermatology 2021
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8273319/
https://www.ncbi.nlm.nih.gov/pubmed/34341640
http://dx.doi.org/10.5021/ad.2021.33.4.369

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8273319/
https://www.ncbi.nlm.nih.gov/pubmed/34341640
http://dx.doi.org/10.5021/ad.2021.33.4.369

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