Keratoderma
Medical condition
From Wikipedia, the free encyclopedia
Keratoderma is a local or general thickening of the horny layer of the epidermis.[1]
| Keratoderma | |
|---|---|
| |
| Diffuse keratodermas affect most of the palms and soles. | |
| Specialty | Dermatology  |
Classification
The keratodermas are classified into the following subgroups:[2]: 506
Congenital
- Simple keratodermas
- Complex keratodermas
- Diffuse palmoplantar keratoderma
- Focal palmoplantar keratoderma
- Ectodermal dysplasias
- Syndromic keratodermas
- Vohwinkel syndrome
- Palmoplantar keratoderma associated with esophageal cancer
- Palmoplantar keratoderma and spastic paraplegia
- Naxos disease
- Striate palmoplantar keratoderma, woolly hair, and left ventricular dilated cardiomyopathy
- Keratitis-ichthyosis-deafness syndrome
- Corneodermatosseous syndrome
- Huriez syndrome
- Oculocutaneous tyrosinemia
- Cardiofaciocutaneous syndrome
- Schöpf–Schulz–Passarge syndrome
Acquired
- Acquired keratodermas
- AIDS-associated keratoderma
- Arsenical keratoses
- Calluses
- Climacteric keratoderma
- Clavi (Corns)
- Eczema
- Human papillomavirus
- Keratoderma blenorrhagicum
- Lichen planus
- Norwegian scabies
- Paraneoplastic keratoderma
- Psoriasis
- Reactive arthritis
- Secondary syphilis
- Tinea pedis
- Sézary syndrome
- Tuberculosis verrucosa cutis
- Drug-induced keratoderma[3]
