A carregar...
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...
Na minha lista:
| Publicado no: | Ann Pediatr Endocrinol Metab |
|---|---|
| Main Authors: | , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
The Korean Society of Pediatric Endocrinology
2015
|
| Assuntos: | |
| Acesso em linha: | 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 |
| Tags: |
Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!
|