| Literature DB >> 31687261 |
Jessika Johannsen1, Tatjana Bierhals2, Philipp Deindl1, Laura Hecher1, Katharina Hermann1, Maja Hempel2, Katja Kloth2, Jonas Denecke1.
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. © Thieme Medical Publishers.Entities:
Keywords: PLPBP (PROSC) gene; seizure cluster; vitamin B6 responsive epilepsy
Year: 2019 PMID: 31687261 PMCID: PMC6824897 DOI: 10.1055/s-0039-1685501
Source DB: PubMed Journal: J Pediatr Genet ISSN: 2146-460X