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229 Possible Causes for Hypocalciuria

  • Muckle Wells Syndrome

    The routine urine-test diagnosed hypocalciuria. Histopathological exams of the skin showed only chronic dermatitis.[]

  • Osteoporosis

    […] calcium/creatinine: Hypercalciuria may be associated with osteoporosis; further investigation with measurement of intact parathyroid hormone and urine pH may be indicated; hypocalciuria[]

  • Bartter's Disease

    […] renal tubular acidosis Hypokalemia Hypochloremia Metabolic alkalosis Normotension Elevated plasma renin level Hypokalemia Hypochloremia Metabolic alkalosis Hypomagnesemia Hypocalciuria[] Indeed, 6 patients (23%) were found to have hypocalciuria. Nozu also reported hypocalciuria in all patients with mutations in the CLCNKB gene.[] Diagnosis of Gitelman syndrome is based on findings similar to Bartter syndrome, as well as on hypomagnesemia, or abnormally low serum concentrations of magnesium , and hypocalciuria[]

  • Hypercalcemia

    Here, we describe a patient with acquired parathyroid hormone (PTH)-dependent hypercalcemia with associated hypocalciuria, found to have true lymphocytic parathyroiditis on[] To evaluate the functional significance of a CaSR mutation, identified in a young infant who presented with hypercalcemia and hypocalciuria.[] In FHH type 2, marked hypocalciuria is noted. FHH type 3 exhibits mild hypophosphatemia and elevated plasma PTH concentrations.[]

  • Primary Hyperparathyroidism

    Gitelman syndrome(GS) is a rare autosomal recessive salt-losing tubulopathy of young adults, characterised by hypokalaemia, hypomagnesaemia, hypocalciuria and secondary hyperaldosteronism[] Reduced calcium excretion at the distal nephron results in hypocalciuria despite high serum calcium levels.[] […] the calcium sensing receptors gene, generating increased levels of serum calcium and reduced sensitivity of the kidney to these increased levels, with resulting relative hypocalciuria[]

  • Hypokalemic Nephropathy

    , Familial Primary Renotubular, Hypokalemia-Hypomagnesemia with Hypocalciuria Familial Hypokalemia-Hypomagnesemia Hypomagnesemia-Hypokalemia, Primary Renotubular, with Hypocalciuria[] […] by high renin, high aldosterone, hypercalciuria, and an abnormal Na -K -2Cl transporter in the thick ascending limb of the loop of Henle, whereas Gitelman syndrome causes hypocalciuria[] Tubular Hypomagnesemia-Hypokalemia with Hypocalcuria Potassium and Magnesium Depletion Primary Renotubular, Hypomagnesemia-Hypokalemia with Hypocalciuria Hypokalemia-Hypomagnesemia[]

  • Idiopathic Hypercalcuria

    CaSR mutations in claudin-16 Distal tubular reabsorption hypoparathyroidism acidosis low vitamin D pseudohypoaldosteronism II [thiazide, amiloride, Gitelman's disease cause hypocalciuria[]

  • Hypoaldosteronism

    Laboratory evaluation disclosed hypokalemia , hypochloremia, hypomagnesemia, alkalosis, hypocalciuria, and a markedly elevated rennin at 2859 ng/mL/h and a suppressed aldosterone[]

  • Hypomagnesemia

    Laboratory tests showed hypokalemia, metabolic alkalosis, hypocalciuria, and hypomagnesemia related to genetically proven GS.[] All patients presented with hypomagnesemia with a high fractional excretion of Mg2 and hypocalciuria.[] IRH is distinguished from the autosomal-dominant form by the lack of hypocalciuria 24.[]

  • Acute Nephritis

    Hypocalciuria was found in the early stages of illness in six patients aged 12 to 30 with acute nephritis.[] The hypocalciuria does not appear to be due to hypocalcaemia, lowered glomerular filtration rate, or hypoparathyroidism.[] It is suggested that the hypocalciuria is due in part to decreased intestinal absorption of calcium, though possibly there is also a primary alteration in renal tubular handling[]

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