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1,726 Possible Causes for Hypomagnesemia, Most Patients Have Adult Onset of Symptoms, Mutation in the CALM2 Gene

  • Gitelman Syndrome

    Laboratory tests showed hypokalemia, metabolic alkalosis, hypocalciuria, and hypomagnesemia related to genetically proven GS.[jrheum.org] Most patients with Gitelman's syndrome have onset of symptoms as adults, but some can present in childhood.[patient.info] Following her admission, intravenous potassium and magnesium supplementation was commenced to counter the observed hypokalemia and hypomagnesemia.[ncbi.nlm.nih.gov]

    Missing: Mutation in the CALM2 Gene
  • Bartter's Disease

    These patients usually have hypocalciuria and hypomagnesemia. Adult patients may have chondrocalcinosis from longstanding hypomagnesemia. II.[clinicaladvisor.com] Most patients with Gitelman's syndrome have onset of symptoms as adults, but some can present in childhood.[patient.info] […] type of genetic inheritance, manifested hypokalemia, metabolic alkalosis, hyperreninemia, hyperplasia juxtaglomerular apparatus (JGA), hyperaldosteronism, in some patients, hypomagnesemia[adc.bmj.com]

    Missing: Mutation in the CALM2 Gene
  • Acute Alcohol Intoxication

    BACKGROUND: Persons with chronic alcoholism frequently have hypocalcemia, hypomagnesemia, and osteoporosis.[ncbi.nlm.nih.gov] Persons with chronic alcoholism frequently have hypocalcemia, hypomagnesemia, and osteoporosis.[nejm.org] Introduction HYPOCALCEMIA and hypomagnesemia are frequently encountered in heavy users of alcohol. 1 2 3 4 5 These changes have been ascribed to concomitant hypoalbuminemia[nejm.org]

    Missing: Most Patients Have Adult Onset of Symptoms Mutation in the CALM2 Gene
  • Chronic Alcoholism

    Hematologic Anemia Leukocytosis or leukopenia Thrombocytopenia Increased serum globulin levels Metabolic Elevated blood ammonia level Hyperglycemia Respiratory alkalosis Hypomagnesemia[clevelandclinicmeded.com]

    Missing: Most Patients Have Adult Onset of Symptoms Mutation in the CALM2 Gene
  • Glycogen Storage Disease due to Muscle Phosphorylase Kinase Deficiency

    The onset of symptoms can occur in childhood or adulthood; most patients have adult onset.[rarediseases.org] There are autosomal recessive forms of GSD IX (caused by mutations in PHKB, PHKG1, PHKG2, CALM1, CALM2, and CALM3 ), a X-linked liver form (caused by mutations in PHKA2 ),[bmcmedgenet.biomedcentral.com] Notably, some individuals with phosphorylase kinase deficiency in muscle do not have any obvious symptoms.[rarediseases.org]

    Missing: Hypomagnesemia
  • Third Trimester Pregnancy

    The concomitant phenomenon of a third trimester pregnancy with a significant degree of pelvic organ prolapse is extremely rare. We report on a patient with pelvic organ prolapse complicating third trimester pregnancy treated by concomitant cesarean hysterectomy and abdominal sacrocolpopexy. A 30-year-old woman,[…][ncbi.nlm.nih.gov]

    Missing: Most Patients Have Adult Onset of Symptoms Mutation in the CALM2 Gene
  • Metabolic Alkalosis

    We report two patients with gentamicin-induced syndrome of hypokalemic metabolic alkalosis and hypomagnesemia.[ncbi.nlm.nih.gov] Most patients with Gitelman's syndrome have onset of symptoms as adults, but some can present in childhood.[patient.info] Hypomagnesemia occurs in only one third of affected individuals. In contrast, hypomagnesemia and hypocalciuria are considered hallmarks of Gitelman's syndrome.[ncbi.nlm.nih.gov]

    Missing: Mutation in the CALM2 Gene
  • Diabetes Mellitus

    BACKGROUND: Type 2 Diabetes Mellitus is a serious metabolic disease that is often associated with vascular complications. There are 1.9 million people living with Diabetes in Ethiopia; diabetes mellitus is found to be the ninth leading cause of death related to its complications. Although the rate of vascular[…][ncbi.nlm.nih.gov]

    Missing: Most Patients Have Adult Onset of Symptoms Mutation in the CALM2 Gene
  • Diarrhea

    Hypomagnesemia after prolonged diarrhea can cause tetany.[merckmanuals.com]

    Missing: Most Patients Have Adult Onset of Symptoms Mutation in the CALM2 Gene
  • Long QT Syndrome

    Acquired long QT syndrome (LQTS) is a disorder of cardiac repolarization most often due to specific drugs, hypokalemia, or hypomagnesemia that may precipitate torsade de pointes[ncbi.nlm.nih.gov] RESULTS: A novel de novo CALM2 mutation (D132H) was discovered by candidate gene screening in a male infant with prenatal bradycardia born to healthy parents.[ncbi.nlm.nih.gov] Electrolyte disturbances: Hypokalemia, Hypomagnesemia, Hypocalcemia.[pedclerk.bsd.uchicago.edu]

    Missing: Most Patients Have Adult Onset of Symptoms

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