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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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| Pubblicato in: | Ann Pediatr Endocrinol Metab |
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| Autori principali: | , , , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
The Korean Society of Pediatric Endocrinology
2015
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4722164/ https://ncbi.nlm.nih.gov/pubmed/26817011 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.6065/apem.2015.20.4.230 |
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