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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...

Celý popis

Uloženo v:
Hlavní autoři: Sanjanaa Srinivasa, Sumedha Ballal, Preetha Tilak, Savitha Murali, Madhukara Jithendriya
Médium: Artigo
Jazyk:Inglês
Vydáno: Wolters Kluwer Medknow Publications 2025-01-01
Edice:Clinical Dermatology Review
Témata:
cathepsin c gene mutation
genetic testing
palmoplantar keratoderma
papillon–lefevre syndrome
periodontitis
On-line přístup:https://journals.lww.com/10.4103/cdr.cdr_60_24
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