A Rare Cause of Seizures: Hypomagnesemia Type 1
Hypomagnesemia type I is a rare autosomal recessive disorder characterized by severe hypomagnesemia, often accompanied by hypocalcemia. This disease is caused by mutations in the TRPM6 gene (which encodes the respective channel), leading to reduced intestinal absorption of magnesium and increased re...
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| Main Authors: | , , , , , |
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| Format: | Book |
| Published: |
Publicações Ciência e Vida,
2023-12-01T00:00:00Z.
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