| KHM | keratoderma hereditaria mutilans |
|---|---|
| GOH | geroderma osteodysplastica hereditaria |
| LH | late healing; lateral hypothalamic [syndrome]; left hand; left heart; left hemisphere; left hyperpho... |
| THH | telangiectasia hereditaria haemorrhagica; trichohyalin |
| PPK | Palmoplantar keratoderma |
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| arthritis mutilans | A form of chronic rheumatoid arthritis in which osteolysis occurs with extensive destruction of the joint cartilages and bony surfaces with pronounced deformities, chiefly of the hands and feet; similar changes can occur in some cases of psoriatic arthritis. (05 Mar 2000) |
|---|---|
| keratoma hereditarium mutilans | Diffuse keratoderma of the extremities, with the development during childhood of constricting fibrous bands around the middle phalanx of the fingers or toes which may lead to spontaneous amputation; autosomal dominant inheritance. Synonym: keratoma hereditarium mutilans, Vohwinkel syndrome. (05 Mar 2000) |
| lupus mutilans | Cutaneous tuberculosis with extensive destruction of tissue. (05 Mar 2000) |
| adynamia episodica hereditaria | Hyperkalaemic periodic paralysis, without myotonia. (05 Mar 2000) |
| porphyria cutanea tarda hereditaria | A form of hepatic porphyria (porphyria, hepatic) characterised by photosensitivity resulting in bullae that rupture easily to form shallow ulcers. This condition occurs in two forms: a sporadic, nonfamilial form that begins in middle age and has normal amounts of uroporphyrinogen decarboxylase with diminished activity in the liver; and a familial form in which there is an autosomal dominant inherited deficiency of uroporphyrinogen decarboxylase in the liver and red blood cells. (12 Dec 1998) |
| protocoproporphyria hereditaria | Porphyria characterised by abdominal pain and neuropsychiatric abnormalities, by dermal sensitivity to light and mechanical trauma, by increased faecal excretion of proto-and coproporphyrin, and by increased urinary excretion of d-aminolevulinic acid, porphobilinogen, and porphyrins; due to a deficiency of protoporphyrinogen oxidase; autosomal dominant inheritance. Synonym: protocoproporphyria hereditaria, South African type porphyria. (05 Mar 2000) |
| syphilis hereditaria | <radiology> Wimberger sign, periostitis, part of ToRCHS complex (12 Dec 1998) |
| syphilis hereditaria tarda | Syphilis, believed to be congenital, but not manifesting itself until several years after birth. (05 Mar 2000) |
| palmoplantar keratoderma | The occurrence of symmetrical diffuse or patchy areas of hypertrophy of the horny layer of the epidermis on the palms and soles; a group of ectodermal dysplasias of considerable variety, and either autosomal dominant or recessive inheritance. Synonym: ichthyosis palmaris et plantaris, keratoderma palmaris et plantaris, keratoderma symmetrica, keratoma plantare sulcatum, keratosis palmaris et plantaris, tylosis palmaris et plantaris. (05 Mar 2000) |
| mutilating keratoderma | Diffuse keratoderma of the extremities, with the development during childhood of constricting fibrous bands around the middle phalanx of the fingers or toes which may lead to spontaneous amputation; autosomal dominant inheritance. Synonym: keratoma hereditarium mutilans, Vohwinkel syndrome. (05 Mar 2000) |
| punctate keratoderma | Horny papules over the palms, soles, and digits that develop central plugs; seen commonly in blacks. Synonym: keratoma disseminatum, keratosis punctata. (05 Mar 2000) |
| senile keratoderma | <dermatology> A skin lesion that is abnormally sensitive to the effects of ultraviolet light (sunlight). Thought to be a precancerous skin lesion that is more common in the fair-skinned or elderly individual. Approximately 20% of these skin lesions will develop into squamous cell carcinoma. Prevention includes the use of sun screen agents and the avoidance of drugs (for example tetracyclines) known to cause photosensitivity reactions. Usually a discreet slightly raised, red or pink lesion located on a sun exposed surface. Texture may appear as rough, gritty or scaly. Growths may be biopsied to look for cancer or removed via cryotherapy or electrical cautery. Some topical agents may be used to promote peeling. (27 Sep 1997) |
| keratoderma | 1. Any horny superficial growth. 2. A generalised thickening of the horny layer of the epidermis. Origin: kerato-+ G. Derma, skin (05 Mar 2000) |
| keratoderma blennorrhagica | Pustules and crusts associated with Reiter's syndrome. Synonym: keratoderma blennorrhagica. (05 Mar 2000) |
| keratoderma blennorrhagicum | The scattered, thickened, hyperkeratotic skin lesions seen in Reiter's syndrome. (05 Mar 2000) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|