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To the Editor: Pseudohypoaldosteronism Type II (PHAII), also known as Gordon syndrome, is a rare autosomal disease, caused by mutations in WNK1, WNK4, CUL3, or KLHL3 genes. Hitherto, about 200… Click to show full abstract
To the Editor: Pseudohypoaldosteronism Type II (PHAII), also known as Gordon syndrome, is a rare autosomal disease, caused by mutations in WNK1, WNK4, CUL3, or KLHL3 genes. Hitherto, about 200 individuals and families have been reported with PHAII; of these, 26 were caused by CUL3 mutation.[1,2] In pediatrics, hyperkalemia‐complicated hypertension is rare, and PHAII should be considered in this condition.
Keywords:
caused cul3;
pseudohypoaldosteronism type;
cul3 mutation
Journal Title: Chinese Medical Journal
Year Published: 2018
Link to full text (if available)
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Journal Title: Chinese Medical Journal
Year Published: 2018
Link to full text (if available)
Share on Social Media: Sign Up to like & get
recommendations!