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.
See also reference (FX) in Slovak
katepsín C
See also reference (FX) in English
Cathepsin C
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subject heading
openseadragon
Number of the records: 1
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