| 영문 | retinitis pigmentosa | 한글 | 색소성망막염 |
|---|---|---|---|
| 설명 | 유전성으로 망막기능의 진행성 소실, 망막위축, 망막혈관 약화, 색소침착, 시야축소 등을 볼 수 있는 망막병. 유전형질은 우성, 열성, X염색체상으로 유전하며, 때로는 다른 유전적 결손과 관련되기도 한다. |
||
| NARP | neuropathy-ataxia-retinitis pigmentosa [syndrome] |
|---|---|
| RP | radial pulse; radiopharmaceutical; rapid processing [of film]; Raynaud phenomenon; reactive protein;... |
| ADRP | Autosomal dominant retinitis pigmentosa |
|---|---|
| ARRP | Autosomal recessive retinitis pigmentosa |
| UP | Urticaria pigmentosa |
| XLRP | X linked retinitis pigmentosa |
| RPGR | retinitis pigmentosa GTP-ase regulator |
| pars pigmentosa | pars pigmentosa |
|---|---|
| retinitis pigmentosa | <ophthalmology> Disease caused by overactivity of the pigmented retinal epithelial cells, leading to damage and occlusion of photoreceptors and blindness. (18 Nov 1997) |
| morphea pigmentosa | Localised scleroderma in which there is an increase in pigmentation. (05 Mar 2000) |
| pseudoretinitis pigmentosa | A widespread pigmentary mottling of the retina that may follow severe eye trauma, especially from a penetrating injury. (05 Mar 2000) |
| dermatopathia pigmentosa reticularis | A persistent purplish network-patterned discoloration of the skin caused by dilation of capillaries and venules due to stasis or changes in underlying blood vessels including hyalinization; rarely appears as a developmental defect. Synonym: angiitis livedo reticularis, dermatopathia pigmentosa reticularis, livedo racemosa. (05 Mar 2000) |
| urticaria pigmentosa | The most common form of mastocytosis. It occurs primarily in children and is typically characterised by multiple persistent small, reddish-brown, hyperpigmented, pruritic macules and papules. They are located most commonly on the trunk, but seen also on the extremities, head, and neck. (12 Dec 1998) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|