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Familial Primary Hypomagnesemia

MedGen UID:
889117
•Concept ID:
C4049202
•
Disease or Syndrome

Definition

A hereditary disorder that leads to a selective defect in renal or intestinal magnesium absorption, resulting in a low serum magnesium concentration. [from NCI]

Term Hierarchy

CClinical test,  RResearch test,  OOMIM,  GGeneReviews,  VClinVar  
  • CROGVFamilial Primary Hypomagnesemia

Professional guidelines

PubMed

Electrolyte disorders with platinum-based chemotherapy: mechanisms, manifestations and management.
Oronsky B, Caroen S, Oronsky A, Dobalian VE, Oronsky N, Lybeck M, Reid TR, Carter CA
Cancer Chemother Pharmacol 2017 Nov;80(5):895-907. Epub 2017 Jul 20 doi: 10.1007/s00280-017-3392-8. PMID: 28730291Free PMC Article
European League Against Rheumatism recommendations for calcium pyrophosphate deposition. Part I: terminology and diagnosis.
Zhang W, Doherty M, Bardin T, Barskova V, Guerne PA, Jansen TL, Leeb BF, Perez-Ruiz F, Pimentao J, Punzi L, Richette P, Sivera F, Uhlig T, Watt I, Pascual E
Ann Rheum Dis 2011 Apr;70(4):563-70. Epub 2011 Jan 7 doi: 10.1136/ard.2010.139105. PMID: 21216817
Diagnosis of hypokalemia: a problem-solving approach to clinical cases.
Assadi F
Iran J Kidney Dis 2008 Jul;2(3):115-22. PMID: 19377223

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