Beyond the Common Causes of Palmoplantar Keratoderma: Papillon–Lefevre Syndrome with a Unique Mutation

Papillon–Lefevre syndrome is a rare autosomal recessive type of syndromic palmoplantar keratoderma, associated with ectodermal dysplasia. It is also known as keratoderma with periodontitis. This condition can cause irreversible loss of dentition with onset in early childhood and predispose to recurr...

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Autors principals:	Sanjanaa Srinivasa, Sumedha Ballal, Preetha Tilak, Savitha Murali, Madhukara Jithendriya
Format:	Artigo
Idioma:	Inglês
Publicat:	Wolters Kluwer Medknow Publications 2025-01-01
Col·lecció:	Clinical Dermatology Review
Matèries:	cathepsin c gene mutation genetic testing palmoplantar keratoderma papillon–lefevre syndrome periodontitis
Accés en línia:	https://journals.lww.com/10.4103/cdr.cdr_60_24
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