ORPHA:678
Papillon-Lefèvre syndrome
Also called Keratosis palmoplantar-periodontopathy syndrome, PLS
- Body system
- Inborn errors of metabolism
- Inheritance pattern
- Autosomal recessive
- Typical age of onset
- Childhood, Infancy, Neonatal
- Estimated prevalence
- 1-9 / 1 000 000 (Worldwide)
- Rarity class
- 1-9 / 1 000 000
ORPHA:678 is classified under "Inborn errors of metabolism" in the Orphanet nomenclature.
Common signs
- Abnormality of the dentition
- Severe periodontitis
- Gingivitis
- Periodontitis
- Palmoplantar hyperkeratosis
- Palmoplantar keratoderma