Diagnosis and Management of Papillon-Lefevre Syndrome: A Rare Case Report and a Brief Review of Literature

Papillon-Lefevre syndrome (PLS) manifests as an autosomal recessive disorder caused by a mutation in the cathepsin C (CTSC) gene. This genetic alteration results in palmoplantar hyperkeratosis, rapid onset of periodontitis, and premature shedding of both primary and permanent teeth. The major etiolo...

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Detalles Bibliográficos
Autores principales: Phull, Tanvi, Jyoti, Divya, Malhotra, Ritu, Nayak, Shanteri, Modi, Himanshi, Singla, Ishu, P, Aishwarrya
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2023
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10493119/
https://www.ncbi.nlm.nih.gov/pubmed/37701012
http://dx.doi.org/10.7759/cureus.43335

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10493119/
https://www.ncbi.nlm.nih.gov/pubmed/37701012
http://dx.doi.org/10.7759/cureus.43335

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