A case report on pseudohypoaldosteronism with a pathogenic mutation of CA12 causes autosomal recessive isolated hyperchlorhidrosis disorder
Pseudohypoaldosteronism (PHA) is a rare genetic condition characterized by the body’s inability to respond properly to the hormone aldosterone, which is essential for regulating sodium and potassium levels, as well as maintaining blood pressure. The aim is to present this case study on the mutation...
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| Format: | Article |
| Language: | English |
| Published: |
Wolters Kluwer Medknow Publications
2025-06-01
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| Series: | Journal of Family Medicine and Primary Care |
| Subjects: | |
| Online Access: | https://journals.lww.com/10.4103/jfmpc.jfmpc_1444_24 |
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