Aetiology
- Hereditary PPK is caused by a mutation in the genes that either code a protein in the keratin
- Can manifest as a sole dermatological disease, i.e. non syndromic or along with extra cutaneous manifestations, i.e. syndromic-i.e. in relation to an inflammatory skin condition (e.g. eczema or psoriasis), systemic inflammatory disease, internal cancers etc.
- Inheritance:
- Autosomal dominant, recessive or X linked.
- Mitochondrial inheritance has also been reported.
Subtypes
- Diffuse keratoderma
- Affects the palms and soles
- Focal keratoderma
- Mainly involves the pressure areas.
- Punctate-type keratoderma
- Causes bumps on the palms and soles.
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