| 영문 | rachitis(=rickets) | 한글 | 구루병 |
|---|---|---|---|
| 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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| LA | lactic acid; large amount; laser angioplasty; late abortion; late antigen; latex agglutination; left... |
|---|---|
| LAR | laryngology; late asthmatic response; late reaction; left arm recumbent; leukocyte antigen-related |
| FHR | familial hypophosphatemic rickets; fetal heart rate |
| HHRH | hereditary hypophosphatemic rickets with hypercalciuria; hypothalamic hypophysiotropic releasing hor... |
| HPDR | hypophosphatemic D-resistant rickets |
| VDRR | Vitamin D resistant rickets |
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| XLH | X-Linked hypophosphataemic rickets |
| HYP | hypophosphataemic rickets |
| AdMLP | Adenovirus major late promoter |
| Ad2MLP | Adenovirus-2 major late promoter |
familial leiomyomatosis cutis et uteri (가족성 피부 자궁 근종증
acute angle
| late rickets | <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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| acute rickets | Bone changes seen in infantile scurvy, consisting of subperiosteal haemorrhage and deficient osteoid tissue formation; often used to indicate simultaneous occurrence of rickets and scurvy. Synonym: acute rickets. Hereditary hypophosphatemic rickets, with hypercalciuria, an inherited disorder in which there is a defect in renal tubular reabsorption. (05 Mar 2000) |
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| adult rickets | <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) |
| refractory rickets | Rickets that does not respond to treatment with usual doses of vitamin D and adequate dietary calcium and phosphorus. Most often due to inherited renal tubular disorder e.g., Fanconi syndrome. Renal rickets, a form of rickets occurring in children in association with and apparently caused by renal disease with hyperphosphatemia. Synonym: pseudorickets, renal fibrocystic osteosis, renal infantilism, renal osteitis fibrosa. (05 Mar 2000) |
| vitamin d-resistant rickets | <radiology> X-linked recessive, defect in renal tubular resorption of phosphate, presents at 1 yr, progressive limb deformities X-ray: less severe changes than other rickets, presents later Differential diagnosis features: family hx, normal serum calcium, marked hypophosphataemia (decreased PO4), no secondary hyperparathyroidism (12 Dec 1998) |
| rickets | <rheumatology, orthopaedics> A condition caused by deficiency of vitamin D, especially in infancy and childhood, with disturbance of normal ossification. The disease is marked by bending and distortion of the bones under muscular action, by the formation of nodular enlargements on the ends and sides of the bones, by delayed closure of the fontanelles, pain in the muscles and sweating of the head. Vitamin D and sunlight together with an adequate diet are curative, provided that the parathyroid glands are functioning properly. Origin: Gr. Rhachitis = a spinal complaint (18 Nov 1997) |
| coeliac rickets | Arrested growth, and osseous deformities associated with defective absorption of fat and calcium in coeliac disease. (05 Mar 2000) |
| haemorrhagic rickets | Bone changes seen in infantile scurvy, consisting of subperiosteal haemorrhage and deficient osteoid tissue formation; often used to indicate simultaneous occurrence of rickets and scurvy. Synonym: acute rickets. Hereditary hypophosphatemic rickets, with hypercalciuria, an inherited disorder in which there is a defect in renal tubular reabsorption. (05 Mar 2000) |
| scurvy rickets | infantile scurvy |
| familial hypophosphatemic rickets | <radiology> X-linked recessive, defect in renal tubular resorption of phosphate, presents at 1 yr, progressive limb deformities X-ray: less severe changes than other rickets, presents later Differential diagnosis features: family hx, normal serum calcium, marked hypophosphataemia (decreased PO4), no secondary hyperparathyroidism (12 Dec 1998) |
| receptors, very late antigen | Members of the integrin family appearing late after T-cell activation. They are a family of proteins initially identified at the surface of stimulated T-cells, but now identified on a variety of cell types. At least six vla antigens have been identified as heterodimeric adhesion receptors consisting of a single common beta-subunit and different alpha-subunits. (12 Dec 1998) |
| late apical systolic murmur | A murmur previously considered benign, or even extracardiac, with a possible relationship to pericardial disease; it often represents mitral insufficiency, often localised and of moderate severity but with propensity for developing bacterial endocarditis, and is frequently associated with systolic click and mitral prolapse (Barlow syndrome; a balloon or billowing mitral valve leaflet) often producing a click, murmur, or both, as it prolapses during systole into the left atrium. (05 Mar 2000) |
| late benign syphilis | Late syphilis, manifested by serologic evidence of infection, but without any clinical manifestations. (05 Mar 2000) |
| late cyanosis | cyanose tardive |
| late deceleration | Any transient foetal bradycardia, the nadir of which occurs after the peak of the uterine contraction. (05 Mar 2000) |
| late diastole | That part of diastole immediately preceding systole. Synonym: late diastole. (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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