Papillon–Lefèvre syndrome: Difference between revisions
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Revision as of 22:11, 16 February 2025
Papillon–Lefèvre syndrome (PLS) is a rare genetic disorder characterized by severe periodontitis leading to premature loss of both primary and permanent teeth, and hyperkeratosis of the palms and soles. It is caused by mutations in the cathepsin C gene.
Symptoms
The primary symptoms of Papillon–Lefèvre syndrome include:
- Periodontitis: This is often the first sign of PLS, usually appearing between the ages of 1 and 4. It leads to inflammation of the gums and eventual loss of teeth.
- Hyperkeratosis: This involves thickening of the skin on the palms of the hands and soles of the feet. It typically develops during the first few years of life.
Causes
Papillon–Lefèvre syndrome is caused by mutations in the cathepsin C gene. This gene provides instructions for making a protein that is involved in the immune system. Mutations in this gene lead to a reduction in the activity of the cathepsin C protein, which impairs the immune system's ability to fight off bacteria in the mouth, leading to periodontitis.
Diagnosis
Diagnosis of Papillon–Lefèvre syndrome is based on the clinical symptoms, particularly the presence of severe periodontitis and hyperkeratosis. Genetic testing can confirm a diagnosis by identifying mutations in the cathepsin C gene.
Treatment
Treatment for Papillon–Lefèvre syndrome primarily involves managing the symptoms. This may include:
- Regular dental cleanings and use of antibacterial mouth rinses to manage periodontitis.
- Use of emollients and keratolytic agents to manage hyperkeratosis.
- Antibiotic therapy to treat any associated infections.
Prognosis
With appropriate management, individuals with Papillon–Lefèvre syndrome can lead normal lives. However, the loss of teeth can affect nutrition and speech, and the skin symptoms can cause discomfort and social stigma.
