Pseudohypoaldosteronism Type 1 with a Novel Mutation in the Gene: A Case Report
Pseudohypoaldosteronism type 1 (PHA1) is a rare salt-wasting disorder caused by resistance to mineralocorticoid action. PHA1 is of two types with different levels of disease severity and phenotype as follows: systemic type with an autosomal recessive inheritance (caused by mutations of the epithelia...
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| Main Authors: | , , , , |
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| Format: | Book |
| Published: |
Korean Society of Pediatric Nephrology,
2020-04-01T00:00:00Z.
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| Online Access: | Connect to this object online. |
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| Call Number: |
A1234.567 |
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| Copy 1 | Available |