Palmoplantar keratoderma is also sometimes known as ‘ keratosis palmaris et plantaris’. Classification of keratodermas depends on whether it is inherited or acquired, and the clinical features. Diffuse keratodermas affect most of the palms and soles.

Type 2: Spiny keratoderma (also known as "Porokeratosis punctata palmaris et plantaris", "Punctate keratoderma", and "Punctate porokeratosis of the palms and soles") is an autosomal dominant keratoderma of late onset that develops in patients aged 12 to 50, characterized by multiple tiny keratotic plugs, resembling the spines on a music box ...

Sep 29, 2022 · Intractable plantar keratosis (IPK) is a discrete, focused callus, usually about 1 cm, on the plantar aspect of the forefoot. Typically, IPKs occur beneath one or more lateral metatarsal heads...

Palmoplantar keratodermas (PPKs) comprise a heterogeneous group of disorders characterized by persistent epidermal thickening of the palms and soles of the skin. Traditionally, PPKs have been...

Aug 26, 2020 · Palmoplantar keratoderma (PPK) is an abnormal thickening of the skin that affects the palms and soles. You can’t cure hereditary PPK, but you can alleviate the symptoms. If you suffer from plantar keratoderma, a consistent foot care routine is a must. An electric callus remover helps keep skin smooth with less irritation.

Inherited monogenic palmoplantar keratodermas are a heterogeneous group of conditions characterised by persistent epidermal thickening of the palmoplantar skin. Palmoplantar keratodermas are grouped depending on the morphology of the keratoderma into diffuse, focal/striate or papular/punctate.

Acquired keratoderma is a palmoplantar keratoderma that is NOT inherited as a primary genetic condition. It may occur as part of a generalised skin condition (some of which may be inherited) or as a result of another illness. How does acquired keratoderma present?

There are three different types of punctate-type keratoderma. Punctate keratoderma: tiny hard rounded bumps in the palms or soles. Some individuals are better classified as having porokeratosis palmaris et plantaris disseminata.

Keratosis palmoplantaris nummularis or hereditary painful callosities is associated with mutation in KRT 6C genes encoding keratin 6c expressed predominantly on plantar skin. It is autosomal dominant and manifests clinically within first 2 years of life as painful, nummular-shaped keratotic plaques located mainly over pressure points.

Palmoplantar keratodermas, also called keratosis palmaris et plantaris or PPKs, are a heterogeneous group of disorders marked by an unusual thickening of the skin on the palms of the hands and soles of the feet.