| 영문 | rachitis(=rickets) | 한글 | 구루병 |
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| 설명 | 비타민D의 부족으로 발생한다. 주로 빛을 많이 쪼이지 못한 어린아이에게서 발생한다. 비타민D는 위창자관에서 칼슘의 흡수를 촉진하고, 오줌으로 칼슘의 분비를 감소시켜, 혈중칼슘농도와 인산염의 농도를 증가시키는 것으로 알려져 있다. 따라서 이것이 부족할 경우 전반적인 뼈의 성장장애로 키가 크지 않고, 구부러진 골격과 쉽게 부서지는 골격을 가지게 된다. 치료는 비타민D의 공급이다. |
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| PCT | 1) Post-Coital Test = Sims-Hubner Test 2) Porp... |
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| PTC | 1) Percutaneous Transhepatic Cholangiography = PTHC ... |
| PCT | peripheral carcinoid tumor; plasma clotting time; plasmacrit test; plasmacytoma; polychlorinated tri... |
| SEDT | spondyloepiphyseal dysplasia tarda |
| SEDT-PA | spondyloepiphyseal dysplasia tarda-progressive arthropathy |
| PCT | Porphyria Cutanea Tarda |
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| rachitis tarda | <pathology> A condition marked by softening of the bones (due to impaired mineralisation, with excess accumulation of osteoid), with pain, tenderness, muscular weakness, anorexia and loss of weight, resulting from deficiency of vitamin D and calcium. Origin: Gr. Malakia = softness (18 Nov 1997) |
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| rachitis | 1. <medicine> Literally, inflammation of the spine, but commonly applied to the rickets. See Rickets. 2. <botany> A disease which produces abortion in the fruit or seeds. Origin: NL, fr. Gr. (sc), fr, the spine Alternative forms: rhachitis. Source: Websters Dictionary (01 Mar 1998) |
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| rachitis foetalis | congenital rickets |
| rachitis foetalis annularis | Congenital enlargement of the epiphyses of the long bones. (05 Mar 2000) |
| rachitis foetalis micromelica | A congenital condition in which development of the long bones is deficient. (05 Mar 2000) |
| rachitis intrauterina | congenital rickets |
| porphyria cutanea tarda | 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) |
| 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) |
| porphyria cutanea tarda symptomatica | 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) |
| neurosis tarda | Neurotic patterns developing in older people, related to organic cerebral lesions. (05 Mar 2000) |
| dentia tarda | Delayed tooth eruption. Origin: L. Delayed (05 Mar 2000) |
| syphilis hereditaria tarda | Syphilis, believed to be congenital, but not manifesting itself until several years after birth. (05 Mar 2000) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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