Hypokalemic periodic paralysis. Presentation of a case
Hypokalemic periodic paralysis is generally caused by autosomal dominant mutations in the voltage-dependent calcium channel gene; seizures of weakness usually persist for hours or days before gradually resolving; the serum potassium level may be low or normal during the crisis. This disorder can pre...
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| Main Authors: | , , |
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| Format: | Book |
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Centro Provincial de Información de Ciencias Médicas. Cienfuegos,
2020-10-01T00:00:00Z.
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| Call Number: |
A1234.567 |
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| Copy 1 | Available |