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174 Possible Causes for Hypocalciuria

  • Osteoporosis

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

  • Muckle Wells Syndrome

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

  • Gitelman Syndrome

    CONCLUSION: Hypovolemia is not the sole cause of hypocalciuria in patients with GS.[] Gitelman syndrome is usually distinguished from Bartter syndrome by the presence of both hypomagnesemia and hypocalciuria.[] His mother had more slight symptoms of weakness than him with mild hypokalemia and hypocalciuria.[]

  • Autosomal Dominant Primary Hypomagnesemia with Hypocalciuria

    Diagnostic methods Diagnosis relies on a hypomagnesemia, hypermagnesuria and hypocalciuria phenotype.[] In a large Dutch family with autosomal dominant renal hypomagnesemia, associated with hypocalciuria, we mapped the disease locus to a 5.6-cM region on chromosome 11q23.[] Gitelman syndrome, familial hypomagnesemia with hypercalciuria and nephrocalcinosis, familial hypomagnesemia with secondary hypocalcemia, autosomal dominant hypomagnesemia with hypocalciuria[]

  • Familal Benign Hypercalcemia

    Benign familial hypocalciuric hypercalcemia is an autosomal dominant condition characterized by lifelong hypercalcemia, relative hypocalciuria, and inappropriately elevated[] We evaluated the role of parathyroid hormone in the relative hypocalciuria of FHH and characterized the renal transport of calcium in this disorder using three previously[] In FHH type 2, marked hypocalciuria is noted. FHH type 3 exhibits mild hypophosphatemia and elevated plasma PTH concentrations.[]

  • Familial Hypocalciuric Hypercalcemia Type 2

    We describe a 65-year-old woman who had hypercalcemia with normal circulating parathyroid hormone concentrations and hypocalciuria, features consistent with FHH, but she did[] Calcium deposits in joints 0000934 Hypercalcemia High blood calcium levels Increased calcium in blood [ more ] 0003072 Hypermagnesemia High blood magnesium levels 0002918 Hypocalciuria[] Benign familial hypocalciuric hypercalcemia (FHH) is an autosomal dominant condition characterized by lifelong hypercalcemia, relative hypocalciuria, and inappropriately elevated[]

  • Neonatal Severe Primary Hyperparathyroidism

    Both parents and one sibling had episodes of hypercalcemia with inappropriately high parathormone levels; in the father there was also relative hypocalciuria consistent with[] NSHPT is characterized by parathyroid hyperplasia, marked and symptomatic PTH-dependent hypercalcemia, relative hypocalciuria, and bone fragility.[] […] parathyroid hormone Neonatal severe primary hyperparathyroidism (NSPH) is a life-threatening condition that presents within days of life with marked hypercalcemia, relative hypocalciuria[]

  • Familial Hypocalciuric Hypercalcemia Type 3

    FHH also causes high levels of parathyroid hormone (PTH) and low levels of calcium in the urine (hypocalciuria).[] Affected individuals have mild or moderate elevations of calcium in serum, relative hypocalciuria, inappropriately normal serum parathyroid levels and may also have increased[] FHH is characterized by hypercalcemia, hypocalciuria, hypermagnesemia, and normal to low levels of parathyroid hormone (PTH).[]

  • 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[]

  • 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.[]

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