| EH | enlarged heart; external hyperalimentation; epidermolytic hyperkeratosis; epoxide hydratase; essenti... |
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| EHK | epidermolytic hyperkeratosis |
| HLP | hepatic lipoperoxidation; hind leg paralysis; holoprosencephaly; hyperkeratosis lenticularis perstan... |
| ACC | accommodation; acetyl coenzyme A carboxylase; acinic cell carcinoma; acute care center; adenoid cyst... |
| AMC | academic medical center; acetylmethyl carbinol; Animal Medical Center; antibody-mediated cytotoxicit... |
| EH | Epidermolytic hyperkeratosis |
|---|---|
| EHK | Epidermolytic hyperkeratosis |
| AHC | Adrenal hypoplasia congenita |
| ACC | Aplasia cutis congenita |
| AMC | Arthrogryposis Multiplex Congenita |
Nd:YAG
| hyperkeratosis congenita | most common form of ichthyosis characterised by prominent scaling especially on the exterior surfaces of the extremities. It is inherited as an autosomal dominant trait. (12 Dec 1998) |
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| generalised epidermolytic hyperkeratosis | Diffusely red, eroded skin at birth, with subsequent scaling, tending to improve in later life, characterised by generalised epidermolytic hyperkeratosis and autosomal dominant inheritance. See: epidermolytic hyperkeratosis. Synonym: generalised epidermolytic hyperkeratosis, ichthyismus hystrix, ichthyosis hystrix. (05 Mar 2000) |
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| hyperkeratosis | 1. Hypertrophy of the corneous layer of the skin. 2a. Any of various conditions marked by hyperkeratosis. 2b. A disease of cattle marked by thickening and wringling of the hide and formation of papillary outgrowths on the buccal mucous membranes, often accompanied by watery discharge from eyes and nose, diarrhoea, loss of condition and abortion of pregnant animals and now believed to result from ingestion of the chlorinated naphthalene of various lubricating oils. (18 Nov 1997) |
| hyperkeratosis eccentrica | A rare, chronic, progressive autosomal dominant disorder seen most often in males and usually appearing in early childhood. It is characterised by the formation of slightly atrophic patches surrounded by an elevated, keratotic border. (12 Dec 1998) |
| hyperkeratosis, epidermolytic | A form of congenital ichthyosis inherited as an autosomal dominant trait and characterised by erythroderma and severe hyperkeratosis. It is manifested at birth by blisters followed by the appearance of thickened, horny, verruciform scales over the entire body, but accentuated in flexural areas. (12 Dec 1998) |
| hyperkeratosis figurata centrifuga atrophica | A rare, chronic, progressive autosomal dominant disorder seen most often in males and usually appearing in early childhood. It is characterised by the formation of slightly atrophic patches surrounded by an elevated, keratotic border. (12 Dec 1998) |
| hyperkeratosis follicularis et parafollicularis | Discrete and confluent horny follicular plugs on a crateriform base, often occurring on the arms and legs in diabetics with renal failure; possibly a severe form of perforating folliculitis. Synonym: hyperkeratosis penetrans, Kyrle's disease. (05 Mar 2000) |
| hyperkeratosis lenticularis perstans | Small keratotic papules on the dorsa of the feet and legs, and occasionally elsewhere, with pinpoint keratotic papules of the palms and soles; onset in the fourth and fifth decades; possibly an autosomal dominant trait. Synonym: Flegel's disease. (05 Mar 2000) |
| hyperkeratosis penetrans | Discrete and confluent horny follicular plugs on a crateriform base, often occurring on the arms and legs in diabetics with renal failure; possibly a severe form of perforating folliculitis. Synonym: hyperkeratosis penetrans, Kyrle's disease. (05 Mar 2000) |
| hyperkeratosis subungualis | Hyperkeratosis affecting the nailbeds of the fingers or toes. (05 Mar 2000) |
| epidermolytic hyperkeratosis | Hyperkeratosis, hypergranulosis, and reticular degeneration in the upper epidermis. Generalised epidermolytic hyperkeratosis is present in bullous congenital ichthyosiform erythroderma. Localised epidermolytic hyperkeratosis may be found in epidermal nevi and benign keratoses. Synonym: porcupine skin. (05 Mar 2000) |
| amaurosis congenita of Leber | An autosomal recessive cone-rod abiotrophy causing blindness or severely reduced vision at birth. (05 Mar 2000) |
| amyoplasia congenita | Limitation of range of joint motion and contractures present at birth, usually involving multiple joints; a syndrome probably of diverse aetiology that may result from changes in spinal cord, muscle, or connective tissue. Several forms exist, autosomal dominant, recessive, and X-linked. Synonym: amyoplasia congenita. (05 Mar 2000) |
| amyotonia congenita | Atonic pseudoparalysis of congenital origin (neither familial nor hereditary), observed especially in infants and characterised by absences of muscular tone only in muscles innervated by the spinal nerves. Synonym: congenital atonic pseudoparalysis, myatonia congenita, Oppenheim's disease, Oppenheim's syndrome. An indefinite term for a number of congenital neuromuscular disorders that cause generalised myotonia in young children, and that have a benign course (static or regressive). (05 Mar 2000) |
| aplasia cutis congenita | Congenital absence or deficiency of a localised area of skin, with the base of the defect covered by a thin translucent membrane; most often a single area near the vertex of the scalp, but may occur in other areas; underlying structures may also be affected; autosomal inheritance, either dominant or recessive. (05 Mar 2000) |
| arthrogryposis multiplex congenita | Limitation of range of joint motion and contractures present at birth, usually involving multiple joints; a syndrome probably of diverse aetiology that may result from changes in spinal cord, muscle, or connective tissue. Several forms exist, autosomal dominant, recessive, and X-linked. Synonym: amyoplasia congenita. (05 Mar 2000) |
| hyperkeratosis congenitalis |
Hyperkeratosis in the harlequin fetus.
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제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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