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Xu, C. Isolated Hyperchlorhidrosis. Encyclopedia. Available online: https://encyclopedia.pub/entry/4199 (accessed on 29 September 2026).
Xu C. Isolated Hyperchlorhidrosis. Encyclopedia. Available at: https://encyclopedia.pub/entry/4199. Accessed September 29, 2026.
Xu, Camila. "Isolated Hyperchlorhidrosis" Encyclopedia, https://encyclopedia.pub/entry/4199 (accessed September 29, 2026).
Xu, C. (2020, December 23). Isolated Hyperchlorhidrosis. In Encyclopedia. https://encyclopedia.pub/entry/4199
Xu, Camila. "Isolated Hyperchlorhidrosis." Encyclopedia. Web. 23 December, 2020.
Isolated Hyperchlorhidrosis
Edit

Isolated hyperchlorhidrosis is characterized by the excessive loss of salt (sodium chloride or NaCl) in sweat.

genetic conditions

References

  1. Chiche J, Ilc K, Laferrière J, Trottier E, Dayan F, Mazure NM, Brahimi-HornMC, Pouysségur J. Hypoxia-inducible carbonic anhydrase IX and XII promote tumorcell growth by counteracting acidosis through the regulation of the intracellularpH. Cancer Res. 2009 Jan 1;69(1):358-68. doi: 10.1158/0008-5472.CAN-08-2470.
  2. Feinstein Y, Yerushalmi B, Loewenthal N, Alkrinawi S, Birk OS, Parvari R,Hershkovitz E. Natural history and clinical manifestations of hyponatremia andhyperchlorhidrosis due to carbonic anhydrase XII deficiency. Horm Res Paediatr.2014;81(5):336-42. doi: 10.1159/000358327.
  3. Feldshtein M, Elkrinawi S, Yerushalmi B, Marcus B, Vullo D, Romi H, Ofir R,Landau D, Sivan S, Supuran CT, Birk OS. Hyperchlorhidrosis caused by homozygousmutation in CA12, encoding carbonic anhydrase XII. Am J Hum Genet. 2010 Nov12;87(5):713-20. doi: 10.1016/j.ajhg.2010.10.008.
  4. Muhammad E, Leventhal N, Parvari G, Hanukoglu A, Hanukoglu I, Chalifa-Caspi V,Feinstein Y, Weinbrand J, Jacoby H, Manor E, Nagar T, Beck JC, Sheffield VC,Hershkovitz E, Parvari R. Autosomal recessive hyponatremia due to isolated saltwasting in sweat associated with a mutation in the active site of CarbonicAnhydrase 12. Hum Genet. 2011 Apr;129(4):397-405. doi: 10.1007/s00439-010-0930-4.
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Entry Collection: MedlinePlus
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Update Date: 23 Dec 2020
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