The clinical and pathological characteristics of a hypokalemic periodic paralysis family with muscle atrophy due to SCN4A R672G mutation and review of literatures
Objective To report a family of hypokalaemic periodic paralysis (HypoPP) with muscle atrophy due to SCN4A gene R672G mutation. The clinical, pathological and MRI characteristics of HypoPP were summarized combining literatures review. Methods and Results The proband was a 27⁃year⁃old male patient who...
| Main Authors: | , , , , |
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| Format: | Article |
| Language: | English |
| Published: |
Tianjin Huanhu Hospital
2022-08-01
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| Series: | Chinese Journal of Contemporary Neurology and Neurosurgery |
| Subjects: | |
| Online Access: | http://www.cjcnn.org/index.php/cjcnn/article/view/2552 |