Pseudohypoaldosteronism type 2
Other Names for this Disease
- Hyperpotassemia and hypertension familial
- Gordon hyperkalemia-hypertension syndrome
- Chloride shunt syndrome
- Familial hyperkalemic hypertension
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On this page
- Bonnardeaux A, Bichet DG. Inherited disorders of the renal tubule. In: Brenner BM ed. Brenner: Brenner and Rector's The Kidney, 8th ed.. Philadelphia, PA: Saunders; 2008;
- Victor RG. Arterial hypertension . In: Goldman L, Ausiello D eds. Goldman: Cecil Medicine, 23rd ed. Philadelphia, PA: Saunders; 2007;
- Ferry RJ. Pseudohypoaldosteronism. eMedicine. 2010; http://emedicine.medscape.com/article/924100-overview. Accessed 12/2/2011.
- Finding Treatment Information - A video developed by GARD Information Specialists that explains how you can find information about treatment for a rare disease.
- GeneReviews provides current, expert-authored, peer-reviewed, full-text articles describing the application of genetic testing to the diagnosis, management, and genetic counseling of patients with specific inherited conditions.
- The Centers for Mendelian Genomics program is working to discover the causes of rare genetic disorders. For more information about applying to the research study, please visit their website.
- Orphanet lists European clinical trials, research studies, and patient registries enrolling people with this condition.
- The Research Portfolio Online Reporting Tool (RePORT) provides access to reports, data, and analyses of research activities at the National Institutes of Health (NIH), including information on NIH expenditures and the results of NIH-supported research. Although these projects may not conduct studies on humans, you may want to contact the investigators to learn more. To search for studies, enter the disease name in the "Text Search" box. Then click "Submit Query".