Excessive Seizure Clusters in an Otherwise Well-Controlled Epilepsy as a Possible Hallmark of Untreated Vitamin B6-Responsive Epilepsy due to a Homozygous PLPBP Missense Variant

Abstract Recently, mutations in the PLPBP gene were described as a novel cause for vitamin B6-responsive epilepsy. We report the outcome in case of a male adolescent with a novel homozygous missense variant in PLPBP who was never treated with pyridoxine until the age of 16 years. He presented with o...

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Veröffentlicht in:Journal of pediatric genetics (Birmingham, Ala.) Ala.), 2019-12, Vol.8 (4), p.222-225
Hauptverfasser: Johannsen, Jessika, Bierhals, Tatjana, Deindl, Philipp, Hecher, Laura, Hermann, Katharina, Hempel, Maja, Kloth, Katja, Denecke, Jonas
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Sprache:eng
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Zusammenfassung:Abstract Recently, mutations in the PLPBP gene were described as a novel cause for vitamin B6-responsive epilepsy. We report the outcome in case of a male adolescent with a novel homozygous missense variant in PLPBP who was never treated with pyridoxine until the age of 16 years. He presented with only mild cognitive impairment and an early-onset, well-controlled epilepsy. In our patient, excessive seizure clusters and anxiety states occurred intermittently, suggesting that the combination might be a hallmark in untreated patients. Thus, mutations in PLPBP should be addressed even in adolescent patients with only mild learning disabilities and relatively good seizure control over the years.
ISSN:2146-4596
2146-460X
DOI:10.1055/s-0039-1685501