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  • hypophosphatemic rickets
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  • hypophosphatemic rickets
    ÀúÀλê(¿°)Ç÷¼º ±¸·çº´(¡­àõ ׬ܻ).
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FHR familial hypophosphatemic rickets; fetal heart rate
HBD has been drinking; hydroxybutyric dehydrogenase; hypophosphatemic bone disease
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...
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  • familial hypophosphatemic rickets

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

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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)
MeSH(Medical Subject Headings) ¸ÂÃã °Ë»ö (http://www.nlm.nih.gov) °á°ú : 1 ÆäÀÌÁö: 1
  • Hypophosphatemic Rickets, X-Linked Dominant - »õâ An X-linked disorder characterized by HYPOPHOSPHATEMIA; RICKETS; OSTEOMALACIA; renal defects in phosphate reabsorption and vitamin D metabolism; and growth retardation. This disorder is caused by mutations in PHEX PHOSPHATE REGULATING NEUTRAL ENDOPEPTIDASE.
    Synonyms : Hypophosphatemia, X-Linked, Vitamin D-Resistant Rickets, X-Linked, X-Linked Hypophosphatemia, Hypophosphatemia, X Linked, Hypophosphatemic Ricket, Hypophosphatemic Rickets, Hypophosphatemic Rickets, X Linked Dominant, Hypophosphatemic Rickets, X-Linked
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hypophosphatemic bone d. an autosomal dominant disorder clinically resembling a mild form of X-linked hypophosphatemia and similarly due to a defect in renal tubular function, but usually showing osteomalacia without radiographic evidence of rickets and responding to calcitriol without supplemental phosphate in at least some cases.
Ãâó: www.mercksource.com/pp/us/cns/cns_health_library.j...
hypophosphatemic r. any of a group of disorders characterized by rickets associated with hypophosphatemia, resulting from dietary phosphorus deficiency (antacid-induced osteomalacia) or due to defects in renal tubular function that may be either hereditary (familial hypophosphatemic rickets) or acquired. While skeletal deformities such as genu varum and short stature are present, neither hypocalcemia, myopathy, nor tetany occur, and serum parathyroid hormone is normal.
Ãâó: www.mercksource.com/pp/us/cns/cns_health_library.j...
hypophosphatemic 1. Having an abnormally low blood phosphate concentration. 2. An agent that lowers the blood phosphate concentration, e.g., in renal failure.
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