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  2. Hyperphosphatemia - Wikipedia

    en.wikipedia.org/wiki/Hyperphosphatemia

    Hyperphosphatemia. Hyperphosphatemia is an electrolyte disorder in which there is an elevated level of phosphate in the blood. [1] Most people have no symptoms while others develop calcium deposits in the soft tissue. [1] The disorder is often accompanied by low calcium blood levels, which can result in muscle spasms.

  3. Sucroferric oxyhydroxide - Wikipedia

    en.wikipedia.org/wiki/Sucroferric_oxyhydroxide

    Sucroferric oxyhydroxide. Sucroferric oxyhydroxide, sold under the brand name Velphoro, is a non-calcium, iron-based phosphate binder used for the control of serum phosphorus levels in adults with chronic kidney disease (CKD) on haemodialysis (HD) or peritoneal dialysis (PD). [6] It is used in form of chewable tablets.

  4. Phosphate binder - Wikipedia

    en.wikipedia.org/wiki/Phosphate_binder

    Phosphate binder. Phosphate binders are medications used to reduce the absorption of dietary phosphate; they are taken along with meals and snacks. They are frequently used in people with chronic kidney failure (CKF), who are less able to excrete phosphate, resulting in an elevated serum phosphate.

  5. Albright's hereditary osteodystrophy - Wikipedia

    en.wikipedia.org/wiki/Albright's_hereditary...

    Phosphate binders, supplementary calcium [ 3 ] Named after. Fuller Albright. Albright's hereditary osteodystrophy is a form of osteodystrophy, [ 4 ] and is classified as the phenotype of pseudohypoparathyroidism type 1A; this is a condition in which the body does not respond to parathyroid hormone. [ 1 ]

  6. Sevelamer - Wikipedia

    en.wikipedia.org/wiki/Sevelamer

    Sevelamer (rINN) is a phosphate binding medication used to treat hyperphosphatemia in patients with chronic kidney disease. When taken with meals, it binds to dietary phosphate and prevents its absorption. Sevelamer was invented and developed by GelTex Pharmaceuticals. Sevelamer is marketed by Sanofi under the brand names Renagel (sevelamer ...

  7. Vitamin D deficiency - Wikipedia

    en.wikipedia.org/wiki/Vitamin_D_deficiency

    Vitamin D deficiency is typically diagnosed by measuring the concentration of the 25-hydroxyvitamin D in the blood, which is the most accurate measure of stores of vitamin D in the body. [1][7][2] One nanogram per millilitre (1 ng/mL) is equivalent to 2.5 nanomoles per litre (2.5 nmol/L). Severe deficiency: <12 ng/mL = <30 nmol/L[2] Deficiency ...

  8. Hypophosphatasia - Wikipedia

    en.wikipedia.org/wiki/Hypophosphatasia

    Rare (1 in 100,000); [3] more common in some populations [4] Hypophosphatasia (/ ˌhaɪpoʊˈfɒsfeɪtˌeɪʒə /; also called deficiency of alkaline phosphatase, phosphoethanolaminuria, [5] or Rathbun's syndrome; [1] sometimes abbreviated HPP[6]) is a rare, and sometimes fatal, inherited [7] metabolic bone disease. [8]

  9. Hyperphosphatasia with mental retardation syndrome - Wikipedia

    en.wikipedia.org/wiki/Hyperphosphatasia_with...

    Other names. Mabry syndrome. This condition is inherited in an autosomal recessive manner. Hyperphosphatasia with mental retardation syndrome, HPMRS, [1] also known as Mabry syndrome, [2] has been described in patients recruited on four continents world-wide. [3] Mabry syndrome was confirmed [4] to represent an autosomal recessive syndrome ...

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