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PedAM

Pediatric Disease Annotations & Medicines




Disease pseudohypoaldosteronism
Phenotype C0020538|hypertension
Sentences 2
PubMedID- 22294159 Background: we found that a mechanism of hypertension in pseudohypoaldosteronism type ii (phaii) caused by a wnk4 missense mutation (d561a) was activation of the wnk-osr1/spak-ncc signal cascade.
PubMedID- 26069767 Her biochemical features mimicked pseudohypoaldosteronism but with initial hypertension, which had not been described in bs.

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