Intractable Generalized Epilepsy and Autosomal Dominant Hypocalcemia: A Case Report
Calcium-sensing receptor gain-of-function mutations are known to cause autosomal dominant hypocalcemia and independently an epilepsy syndrome. We report the unique case of a child with both intractable generalized epilepsy and a chronic abnormality in calcium homeostasis due to a calcium-sensing rec...
| Main Authors: | , , , |
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| Format: | Article |
| Language: | English |
| Published: |
SAGE Publishing
2019-09-01
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| Series: | Child Neurology Open |
| Online Access: | https://doi.org/10.1177/2329048X19876199 |