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Type-5 Bartter syndrome presenting with metabolic seizure in adulthood
Bartter syndrome is a very rare and heterogeneous disease with variable age of onset and symptom severity. Genotypically they have inherited disorders of the thick ascending limb in the renal tubular system, which manifest phenotypically as electrolyte imbalance due to loss of sodium, chloride and p...
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| Publicado no: | BMJ Case Rep |
|---|---|
| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BMJ Publishing Group
2021
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7893602/ https://ncbi.nlm.nih.gov/pubmed/33597159 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/bcr-2020-235349 |
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