Hypokalemic Periodic Paralysis: Narrative Review
Hypokalemic periodic paralysis is a rare genetic pathology characterized by spontaneous muscle weakness up to paralysis along with hypokalemia. The disease development is associated with changes in the CACNA1S, SCN4A, KCNJ2, and KCNJ18 genes regulating ion channels functioning in skeletal muscle cel...
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| Päätekijät: | , , |
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| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
"Paediatrician" Publishers LLC
2026-02-01
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| Sarja: | Вопросы современной педиатрии |
| Aiheet: | |
| Linkit: | https://vsp.spr-journal.ru/jour/article/view/3926 |
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