A Case of Pyridoxine Dependent Epilepsy Presented with Status Epilepticus
Pyridoxine-dependent epilepsy (PDE) is a rare autosomal recessive encephalopathy due to mutations in the ALDH7A1 gene. Intractable seizures are the most frequent clinical form in the early infantile period. A case of a 4-month-old female patient presented to our hospital with status epilepticus. Her...
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Main Authors: | Senem Ayça (Author), Hamide Betül Gerik Çelebi (Author), Sırrı Çam (Author), Muzaffer Polat (Author) |
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Format: | Book |
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Galenos Yayinevi,
2019-04-01T00:00:00Z.
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