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Papillonova-Lefevreova choroba
Record number d010214 Date 06.06.2025 Type M - MESH Topical term Papillonova-Lefevreova choroba See also (Skutočné meno) katepsín C
UDC C16.320.850.475.600C17.800.428.435.600C17.800.827.475.600 Note Rare, autosomal recessive disorder occurring between the first and fifth years of life. It is characterized by palmoplantar keratoderma with periodontitis followed by the premature shedding of both deciduous and permanent teeth. Mutations in the gene for CATHEPSIN C have been associated with this disease. 
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Number of the records: 1