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¿µ¹® rachitis(=rickets) ÇÑ±Û ±¸·çº´
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  • ¿µ¹®
    ÇѱÛ
  • fetal rickets
    žƱ¸·çº´
  • hypophosphatemic rickets
    ÀúÀλêÇ÷±¸·çº´
  • hepatic rickets
    °£¼º±¸·çº´
  • oncogenous rickets
    Á¾¾ç¼º±¸·çº´
  • refractory rickets
    ºñŸ¹ÎDºÒÀÀ±¸·çº´, ºÒÀÀ¼º±¸·çº´
  • renal rickets
    ÄáÆÏ±¸·çº´, ½ÅÀ强±¸·çº´
  • rickets
    ±¸·çº´
  • vitamin D-dependent rickets
    ºñŸ¹ÎDÀÇÁ¸±¸·çº´
  • vitamin D-resistant rickets
    ºñŸ¹ÎDÀúÇ×±¸·çº´
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  • rickets
    ±¸·çº´
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  • fetal rickets
    žƱ¸·íº´
  • hepatic rickets
    °£Å¿±¸·íº´
  • hypophosphatemic rickets
    ÀúÀλêÇ÷¼º±¸·íº´
  • oncogenous rickets
    Á¾¾ç±¸·íº´
  • rickets
    ±¸·íº´
  • refractory rickets
    (¢¡vitamin D-resistant rickets) ºñŸ¹ÎµðÀúÇ×±¸·íº´
  • renal rickets
    ÄáÆÏ±¸·íº´, ½ÅÀ屸·íº´
  • vitamin D-dependent rickets
    ºñŸ¹ÎµðÀÇÁ¸±¸·íº´
  • vitamin D-resistant rickets
    ºñŸ¹ÎµðÀúÇ×±¸·íº´
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  • Glissonian rickets
    ±Û¸®½¼±¸·çº´.
  • Glissonian rickets
    ±Û¸®½¼ ±¸·çº´.
  • hemorrhagic rickets
    ÃâÇ÷(¼º) ±¸·çº´.
  • hepatic rickets
    °£¼º±¸·çº´(¡­ תܻ).
  • hepatic rickets
    °£¼º ±¸·çº´(¡­ תܻ).
  • hypophosphatemic rickets
    ÀúÀλê(¿°)Ç÷¼º ±¸·çº´(¡­àõ ׬ܻ).
  • infantile rickets
    ¿µ¾Æ±¸·çº´(?ä® ×§Ü»).
  • refractory rickets
    ³­Ä¡±¸·çº´(Ññö½ ׬ܻ).
  • refractory rickets
    ³­Ä¡±¸·çº´(Ññö½ ׬ܻ)
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  • early rickets
    Á¶±â±¸·çº´(¡­ ×§Ü»).
  • fat rickets
    Áö¹æ ±¸·çº´(ò·Û¸ ±¸·çÜ»), ºñ¸¸¼º ±¸·çº´.
  • fetal rickets
    žƱ¸·çº´.
  • florid rickets
    °³È­¼º ±¸·çº´(ËÒü£àõ תܻ).
  • hemorrhagic rickets
    ÃâÇ÷(¼º) ±¸·çº´.
  • hepatic rickets
    °£¼º ±¸·çº´(¡­ תܻ).
  • hepatic rickets
    °£¼º±¸·çº´(¡­ תܻ).
  • hypophosphatemic rickets
    ÀúÀλê(¿°)Ç÷¼º ±¸·çº´(¡­àõ ׬ܻ).
  • infantile rickets
    ¿µ¾Æ±¸·çº´(?ä® ×§Ü»).
  • late rickets
    ¸¸¹ß±¸·çº´.
  • late rickets
    ¸¸¹ß ±¸·çº´.
  • refractory rickets
    ³­Ä¡±¸·çº´(Ññö½ ׬ܻ).
  • refractory rickets
    ³­Ä¡±¸·çº´(Ññö½ ׬ܻ)
  • renal rickets
    ½Å¼º±¸·çº´
  • renal rickets
    ½Å¼º ±¸·çº´(ãìàõ ץܻ).
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  • adult rickets
    ¼ºÀÎ ±¸·çº´ (à÷ìÑϣץܻ)
  • rickets
    ±¸·çº´(ϣץܻ)
  • vitamin D-resistant rickets
    ºñŸ¹Î D ÀúÇ×¼º(î½ù÷àõ) ±¸·çº´(±¸·çÜ»)
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  • renal rickets
    ½Å¼º ±¸·çº´
  • rickets
    ±¸·çº´
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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...
HVDRR hypocalcemic vitamin D-resistant rickets
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Pd Pseudodeficiency
VDRR Vitamin D resistant rickets
XLH X-Linked hypophosphataemic rickets
HYP hypophosphataemic rickets
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  • adult rickets
    °ñ¿¬È­Áõ
    ¸ðµç ÁöÁö°ñÀÇ ½ÉÇÑ ±âÇü°ú °ñÀý.
  • familial hypophosphatemic rickets

    familial leiomyomatosis cutis et uteri (°¡Á·¼º ÇǺΠÀڱà ±ÙÁ¾Áõ

  • renal rickets
    ½Å¼º ±¸·çº´
  • rickets
    ±¸·çº´
    ºñŸ¹Î DÀÇ °áÇÌÀÌ ¿øÀÎÀ¸·Î Á¤»óÀûÀÎ »À Çü¼ºÀÌ Àå¾ÖµÇ´Â °ÍÀ¸·Î, ƯÈ÷ Á¥¸ÔÀÌ, À¯¾Æ¿¡¼­ ÀÚÁÖ º¼ ¼ö ÀÖ´Ù. ±ÙÀ° ¿îµ¿¿¡ ÀÇÇÏ¿© »ÀÀÇ ±¼°îÀÌ »ý±â¸ç, °ñ´Ü, °ñ ¿¬°ñºÎ¿¡ °áÀý»óÀÇ Á¾Ã¢À» º¼ ¼ö ÀÖÀ¸¸ç, õ±ÃÀÇ Æó¼â°¡ ´Ê¾î ±ÙÀ°Åë, µÎºÎ ¹ßÇÑ µîÀ» Ư¡ÀûÀ¸·Î º¼ ¼ö ÀÖ´Ù. ºÎ°©»ó¼± ±â´ÉÀÌ Á¤»óÀ̸é, Ư¼öÇÑ ½Ä¹° ¼·Ãë¿Í ºñŸ¹Î D Åõ¿© ¹× Àϱ¤¿å¿¡ ÀÇÇÏ¿© Ä¡À¯µÈ´Ù.
  • vit D-resistant rickets
    D-ÀúÇ×¼º ±¸·çº´
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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)
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)
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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