| 释义 |
- Classification Congenital Acquired
- See also
- References
- External links
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}}Keratoderma is a hornlike skin condition.[1] Classification The keratodermas are classified into the following subgroups:[2]{{rp|506}} Congenital- Simple keratodermas
- Diffuse palmoplantar keratodermas
- Diffuse epidermolytic palmoplantar keratoderma
- Diffuse nonepidermolytic palmoplantar keratoderma
- mal de Meleda
- Focal palmoplantar keratoderma
- Striate palmoplantar keratoderma
- Punctate palmoplantar keratoderma
- Keratosis punctata palmaris et plantaris
- Spiny keratoderma
- Focal acral hyperkeratosis
- Complex keratodermas
- Diffuse palmoplantar keratoderma
- Erythrokeratodermia variabilis
- Palmoplantar keratoderma of Sybert
- Olmsted syndrome
- Naegeli–Franceschetti–Jadassohn syndrome
- Focal palmoplantar keratoderma
- Papillon–Lefèvre syndrome
- Pachyonychia congenita type I
- Pachyonychia congenita type II
- Focal palmoplantar keratoderma with oral mucosal hyperkeratosis
- Camisa disease
- Ectodermal dysplasias
- Clouston's hidrotic ectodermal dysplasia
- Acrokeratotic poikiloderma
- Dermatopathic pigmentosa reticularis
- 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]
See also- Palmoplantar keratoderma
- Skin lesion
- List of cutaneous conditions
- List of conditions caused by problems with junctional proteins
References1. ^WordNet Search - 3.0
2. ^Freedberg, et al. (2003). Fitzpatrick's Dermatology in General Medicine. (6th ed.). McGraw-Hill. {{ISBN|0-07-138076-0}}.
3. ^{{cite book |author=Rapini, Ronald P. |author2=Bolognia, Jean L. |author3=Jorizzo, Joseph L. |title=Dermatology: 2-Volume Set |publisher=Mosby |location=St. Louis |year=2007 |pages=778 |isbn=1-4160-2999-0 |oclc= |doi= |accessdate=}}
External links {{Medical resources
| ICD10 = {{ICD10|L|85|1|l|80}}, {{ICD10|L|86||l|80}}, {{ICD10|Q|82|8|q|80}}
}}{{Cutaneous ketatosis, ulcer, atrophy, and necrobiosis}}{{Congenital malformations and deformations of integument}}{{Cutaneous-condition-stub}} 1 : Papulosquamous hyperkeratotic cutaneous conditions |