Gitelman syndrome combined with growth hormone deficiency
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DOI: 10.1097/md.0000000000017244
Abstract: Abstract Rationale: Gitelman syndrome (GS) is a rare autosomal recessive hereditary salt-losing tubulopathy caused by loss-of-function mutations in the SLC12A3 gene. It is usually characterized by hypokalemia, metabolic alkalosis, hypomagnesemia, and hypocalciuria. There are only… read more here.
Keywords: gitelman syndrome; growth; hormone deficiency; growth hormone ... See more keywords