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Papillon Lefevre Syndrome.
Indian Journal of Dermatology, Venereology and Leprology
|March 8, 2017
Summary
This report details a rare case of Papillon-Lefevre syndrome, a genetic disorder. Early diagnosis and management are crucial for patients with this condition.
Area of Science:
- Genetics
- Dermatology
- Oral Medicine
Background:
- Papillon-Lefevre syndrome is an autosomal recessive disorder.
- Characterized by palmoplantar hyperkeratosis and periodontitis.
Observation:
- A case presentation of Papillon-Lefevre syndrome is described.
- The report focuses on the clinical manifestations and diagnostic features.
Findings:
- The syndrome presents with severe, rapidly progressing periodontitis leading to premature tooth loss.
- Distinctive skin changes, particularly hyperkeratosis on palms and soles, are observed.
Implications:
- Highlights the importance of recognizing rare genetic syndromes.
- Emphasizes the need for multidisciplinary management involving dentists, dermatologists, and geneticists.
- Contributes to the understanding of Papillon-Lefevre syndrome's clinical spectrum.
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