ALLMedicine™ Autosomal Dominant Pseudohypoaldosteronism Type 1 Center
Research & Reviews 2 results
https://rarediseases.info.nih.gov/diseases/9145/autosomal-dominant-pseudohypoaldosteronism-type-1
Dec 1st, 2011 - Autosomal dominant pseudohypoaldosteronism type 1 is a disorder of electrolyte metabolism characterized by excess loss of salt in the urine, failure to thrive and dehydration. Patients typically present in the newborn period, improve with age, and...
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2779785
BMC Nephrology; Kanda K, Nozu K et. al.
Nov 16th, 2009 - Autosomal dominant pseudohypoaldosteronism type 1 (PHA1) is a rare inherited condition that is characterized by renal resistance to aldosterone as well as salt wasting, hyperkalemia, and metabolic acidosis. Renal PHA1 is caused by mutations of the...
Clinicaltrials.gov 2 results
https://rarediseases.info.nih.gov/diseases/9145/autosomal-dominant-pseudohypoaldosteronism-type-1
Dec 1st, 2011 - Autosomal dominant pseudohypoaldosteronism type 1 is a disorder of electrolyte metabolism characterized by excess loss of salt in the urine, failure to thrive and dehydration. Patients typically present in the newborn period, improve with age, and...
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2779785
BMC Nephrology; Kanda K, Nozu K et. al.
Nov 16th, 2009 - Autosomal dominant pseudohypoaldosteronism type 1 (PHA1) is a rare inherited condition that is characterized by renal resistance to aldosterone as well as salt wasting, hyperkalemia, and metabolic acidosis. Renal PHA1 is caused by mutations of the...
