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Gitelman syndrome (medical condition): A rare, relatively mild, genetic kidney disorder...more »
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Gitelman syndrome:
»Introduction: Gitelman syndrome
»Symptoms of Gitelman syndrome
Gitelman syndrome: a disorder seen in older children and young adults characterized by hypokalemia, hypomagnesemia, hypocalciuria, and sometimes tetany.
Source: Stedman's Medical Spellchecker, © 2006 Lippincott Williams & Wilkins. All rights reserved.
Gitelman syndrome: An inherited renal disorder characterized by defective NaCl reabsorption in the convoluted DISTAL KIDNEY TUBULE leading to HYPOKALEMIA. In contrast with BARTTER SYNDROME, Gitelman syndrome includes hypomagnesemia and normocalcemic hypocalciuria and is caused by mutations in the thiazide-sensitive SODIUM CHLORIDE COTRANSPORTER.
Source: MeSH 2007
These medical condition or symptom topics may be relevant to medical information for Gitelman syndrome:
Gitelman syndrome is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Gitelman syndrome, or a subtype of Gitelman syndrome,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
Ophanet, a consortium of European partners,
currently defines a condition rare when if affects 1 person per 2,000.
They list Gitelman syndrome as a "rare disease".
Source - Orphanet
Gitelman syndrome (medical condition): See Gitelman syndrome (disease information).
»Introduction: Gitelman syndrome
»Symptoms of Gitelman syndrome
Gitelman syndrome: Gitelman syndrome is listed as a type of (or associated with) the following medical conditions in our database:
These medical disease topics may be related to Gitelman syndrome:
Source: Diseases Database
Source - NIH
Source: Diseases Database
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