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Papillonova-Lefevreova choroba
Č. záznamu d010214 Dátum 06.06.2025 Typ M - MESH Tematický termín Papillonova-Lefevreova choroba Pozri tiež (Skutočné meno) katepsín C
MDT C16.320.850.475.600C17.800.428.435.600C17.800.827.475.600 Poznámka 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. predmetové heslo
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