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About 4 results

ALLMedicine™ Autosomal Dominant Pseudohypoaldosteronism Type 1 Center

Research & Reviews  2 results

Autosomal dominant pseudohypoaldosteronism type 1
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...

Autosomal dominant pseudohypoaldosteronism type 1 with a novel splice site mutation in ...
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...

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Clinicaltrials.gov  2 results

Autosomal dominant pseudohypoaldosteronism type 1
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...

Autosomal dominant pseudohypoaldosteronism type 1 with a novel splice site mutation in ...
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...

see more →