| ¿µ¹® | scurvy | ÇÑ±Û | ±«Ç÷º´ |
|---|---|---|---|
| ¼³¸í | ºñŸ¹Î CÀÇ °áÇÌÀ¸·Î »ý±â´Â º´. À½½Ä¹° ¼ÓÀÇ ºñŸ¹Î CºÎÁ·, âÀÚ°üÀÇ Èí¼öÀå¾Ö, ¼¼±Õ°¨¿°À¸·Î ÀÎÇÑ Ã¼³» ¼ö¿ä·®ÀÇ ¾ÓÁø µîÀÌ ¿øÀÎÀ¸·Î ¹ßº´ÇÑ´Ù. Áõ»óÀÇ Æ¯Â¡Àº ÃâÇ÷°ú »ÀÀÇ º¯ÁúÀ̸ç, ¼¼È÷ ³ªÅ¸³´Ù. Ãʱ⿡´Â Àü½ÅÀÇ ±ÇÅÂ¿Í ¹«·Â°¨, ½Ä¿åºÎÁø, ·ù¸¶Æ¼½º°°Àº µ¿Åë, ÃâÇ÷¼º ¼ÒÀÎÀÌ ÀÎÁ¤µÈ´Ù. ÀÌ¾î¼ ±¸°Á¡¸·-ÇÇÇÏ-±ÙÀ°-°ñ¸·ÇÏ-³»Àå µî¿¡ ÃâÇ÷·Î ÀÎÇÑ Ç÷Á¾ÀÌ ³ªÅ¸³´Ù. ÁßÁõÀº °íµµÀÇ ºóÇ÷-Ä«Äʽþƿ¡ ºüÁø´Ù. »ýÈÄ 6°³¿ù ÀÌÈÄÀÇ Àΰø¿µ¾ç¾Æ¿¡¼ ÁÖ·Î º¼ ¼ö ÀÖ´Â À¯¾Æ±«Ç÷º´Àº ¼ºÀÎÀÇ °æ¿ì¿Í ´Ù¼Ò ´Þ¶ó¼, À̰ÍÀ» ±âÀçÇÑ µ¶ÀÏ ¹× ¿µ±¹ ÀÇ»çÀÇ À̸§À» µû¼ ƯÈ÷ ¹¢·¯-¹ß·Îº´(Moller-Barlow disease)À̶ó ºÎ¸¥´Ù. üÁßÀÇ Áõ°¡µµ Á¤ÁöµÇ°í ¿µ¾ç»óŵµ ºÒ·®ÇØÁø´Ù. Ä¡·á´Â ºñŸ¹Î C¸¦ ´ë·® Åõ¿©ÇÑ´Ù. |
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| ¿µ¹® | rachitis(=rickets) | ÇÑ±Û | ±¸·çº´ |
|---|---|---|---|
| ¼³¸í | ºñŸ¹ÎDÀÇ ºÎÁ·À¸·Î ¹ß»ýÇÑ´Ù. ÁÖ·Î ºûÀ» ¸¹ÀÌ ÂÉÀÌÁö ¸øÇÑ ¾î¸°¾ÆÀÌ¿¡°Ô¼ ¹ß»ýÇÑ´Ù. ºñŸ¹ÎD´Â À§Ã¢ÀÚ°ü¿¡¼ Ä®½·ÀÇ Èí¼ö¸¦ ÃËÁøÇϰí, ¿ÀÁÜÀ¸·Î Ä®½·ÀÇ ºÐºñ¸¦ °¨¼Ò½ÃÄÑ, Ç÷ÁßÄ®½·³óµµ¿Í Àλ꿰ÀÇ ³óµµ¸¦ Áõ°¡½ÃŰ´Â °ÍÀ¸·Î ¾Ë·ÁÁ® ÀÖ´Ù. µû¶ó¼ À̰ÍÀÌ ºÎÁ·ÇÒ °æ¿ì Àü¹ÝÀûÀÎ »ÀÀÇ ¼ºÀåÀå¾Ö·Î ۰¡ Å©Áö ¾Ê°í, ±¸ºÎ·¯Áø °ñ°Ý°ú ½±°Ô ºÎ¼Áö´Â °ñ°ÝÀ» °¡Áö°Ô µÈ´Ù. Ä¡·á´Â ºñŸ¹ÎDÀÇ °ø±ÞÀÌ´Ù. |
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| CSS | Cancer Surveillance System; carotid sinus stimulation; carotid sinus syndrome; cavernous sinus syndr... |
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| FHR | familial hypophosphatemic rickets; fetal heart rate |
| HHRH | hereditary hypophosphatemic rickets with hypercalciuria; hypothalamic hypophysiotropic releasing hor... |
| HPDR | hypophosphatemic D-resistant rickets |
| HR | heart rate; hemorrhagic retinopathy; high resolution; higher rate; histamine receptor; hormonal resp... |
| VDRR | Vitamin D resistant rickets |
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| XLH | X-Linked hypophosphataemic rickets |
| HYP | hypophosphataemic rickets |
familial leiomyomatosis cutis et uteri (°¡Á·¼º ÇǺΠÀڱà ±ÙÁ¾Áõ
| scurvy rickets | infantile scurvy |
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| Alpine scurvy | <disease> A niacin deficiency disease (pellagra) caused by improper diet and characterised by skin lesions, gastrointestinal disturbances and nervousness. Depression, dermatitis, dementia and diarrhoea are common symptoms. (27 Sep 1997) |
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| haemorrhagic scurvy | Scurvy with extensive haemorrhages in gums, skin and other tissues, typical of severe stage of the disease. Infantile scurvy, osteopathia haemorrhagia infantum;a cachectic condition in infants, resulting from malnutrition and marked by pallor, fetid breath, coated tongue, diarrhoea, and subperiosteal haemorrhages; probably a combination of scurvy and rickets due to combined deficiency of vitamins C and D. Synonym: Barlow's disease, Cheadle's disease, osteopathia haemorrhagica infantum, scurvy rickets. Land scurvy, formerly, scurvy occurring in people who had not been to sea. (05 Mar 2000) |
| scurvy | Disease caused by Vitamin C deficiency. The effects are due to a failure of the hydroxylation of proline residues in collagen synthesis and the consequent failure of fibroblasts to produce mature collagen. See: hydroxyproline. (18 Nov 1997) |
| sea scurvy | Disease caused by Vitamin C deficiency. The effects are due to a failure of the hydroxylation of proline residues in collagen synthesis and the consequent failure of fibroblasts to produce mature collagen. See: hydroxyproline. (18 Nov 1997) |
| trummerfeld scurvy zone | <radiology> Lucent band in metaphysis beneath white line of Frankel, seen in scurvy (12 Dec 1998) |
| 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) |
| 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) |
| 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) |
| 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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