Pseudohypoaldosteronism in a newborn male with functional polymorphisms in the mineralocorticoid receptor genes
Hyponatremia and hyperkalemia in infancy can be attributed to various causes, originating from a variety of renal and genetic disorders. Pseudohypoaldosteronism type 1 (PHA1) is one of these disorders, causing mineralocorticoid resistance that results in urinary salt wasting, failure to thrive, meta...
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| Main Authors: | , , , , , , |
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| Format: | Book |
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Korean Society of Pediatric Endocrinology,
2015-12-01T00:00:00Z.
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