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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[emedicine.medscape.com]

  • Muckle Wells Syndrome

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

  • Gitelman Syndrome

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

  • Autosomal Dominant Primary Hypomagnesemia with Hypocalciuria

    Diagnostic methods Diagnosis relies on a hypomagnesemia, hypermagnesuria and hypocalciuria phenotype.[orpha.net] 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.[ncbi.nlm.nih.gov] Gitelman syndrome, familial hypomagnesemia with hypercalciuria and nephrocalcinosis, familial hypomagnesemia with secondary hypocalcemia, autosomal dominant hypomagnesemia with hypocalciuria[wwww.unboundmedicine.com]

  • Familal Benign Hypercalcemia

    Benign familial hypocalciuric hypercalcemia is an autosomal dominant condition characterized by lifelong hypercalcemia, relative hypocalciuria, and inappropriately elevated[uthealth.influuent.utsystem.edu] 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[scinapse.io] In FHH type 2, marked hypocalciuria is noted. FHH type 3 exhibits mild hypophosphatemia and elevated plasma PTH concentrations.[orpha.net]

  • 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[uir.ulster.ac.uk] Calcium deposits in joints 0000934 Hypercalcemia High blood calcium levels Increased calcium in blood [ more ] 0003072 Hypermagnesemia High blood magnesium levels 0002918 Hypocalciuria[rarediseases.info.nih.gov] Benign familial hypocalciuric hypercalcemia (FHH) is an autosomal dominant condition characterized by lifelong hypercalcemia, relative hypocalciuria, and inappropriately elevated[shifrinmd.com]

  • 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[ncbi.nlm.nih.gov] NSHPT is characterized by parathyroid hyperplasia, marked and symptomatic PTH-dependent hypercalcemia, relative hypocalciuria, and bone fragility.[iofbonehealth.org] […] parathyroid hormone Neonatal severe primary hyperparathyroidism (NSPH) is a life-threatening condition that presents within days of life with marked hypercalcemia, relative hypocalciuria[pediatrics.aappublications.org]

  • Familial Hypocalciuric Hypercalcemia Type 3

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

  • Bartter's Disease

    […] renal tubular acidosis Hypokalemia Hypochloremia Metabolic alkalosis Normotension Elevated plasma renin level Hypokalemia Hypochloremia Metabolic alkalosis Hypomagnesemia Hypocalciuria[medbullets.com] Indeed, 6 patients (23%) were found to have hypocalciuria. Nozu also reported hypocalciuria in all patients with mutations in the CLCNKB gene.[journals.plos.org] 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[britannica.com]

  • Hypomagnesemia

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

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