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Dramatic response after functional hemispherectomy in a patient with epileptic encephalopathy carrying a de novo COL4A1 mutation.
Hino-Fukuyo, Naomi; Kikuchi, Atsuo; Iwasaki, Masaki; Sato, Yuko; Kubota, Yuki; Kobayashi, Tomoko; Nakayama, Tojo; Haginoya, Kazuhiro; Arai-Ichinoi, Natsuko; Niihori, Tetsuya; Sato, Ryo; Suzuki, Tasuku; Kudo, Hiroki; Funayama, Ryo; Nakayama, Keiko; Aoki, Yoko; Kure, Shigeo.
Afiliación
  • Hino-Fukuyo N; Center for Genomic Medicine, Tohoku University Hospital, Sendai, Japan; Department of Pediatrics, Tohoku University School of Medicine, Sendai, Japan. Electronic address: naomi-h@zc4.so-net.ne.jp.
  • Kikuchi A; Department of Pediatrics, Tohoku University School of Medicine, Sendai, Japan.
  • Iwasaki M; Department of Neurosurgery, National Center Hospital of Neurology and Psychiatry, Kodaira, Tokyo, Japan.
  • Sato Y; Department of Pediatrics, Tohoku University School of Medicine, Sendai, Japan.
  • Kubota Y; Department of Pediatrics, Tohoku University School of Medicine, Sendai, Japan.
  • Kobayashi T; Department of Pediatrics, Tohoku University School of Medicine, Sendai, Japan.
  • Nakayama T; Department of Pediatrics, Tohoku University School of Medicine, Sendai, Japan.
  • Haginoya K; Department of Pediatrics, Tohoku University School of Medicine, Sendai, Japan; Department of Neurology, Miyagi Children's Hospital, Sendai, Japan.
  • Arai-Ichinoi N; Department of Pediatrics, Tohoku University School of Medicine, Sendai, Japan.
  • Niihori T; Center for Genomic Medicine, Tohoku University Hospital, Sendai, Japan; Department of Medical Genetics, Tohoku University School of Medicine, Sendai, Japan.
  • Sato R; Department of Pediatrics, Tohoku University School of Medicine, Sendai, Japan.
  • Suzuki T; Department of Pediatrics, Tohoku University School of Medicine, Sendai, Japan.
  • Kudo H; Department of Pediatrics, Tohoku University School of Medicine, Sendai, Japan.
  • Funayama R; Division of Cell Proliferation, United Center for Advanced Research and Translational Medicine, Tohoku University School of Medicine, Sendai, Japan.
  • Nakayama K; Division of Cell Proliferation, United Center for Advanced Research and Translational Medicine, Tohoku University School of Medicine, Sendai, Japan.
  • Aoki Y; Center for Genomic Medicine, Tohoku University Hospital, Sendai, Japan; Department of Medical Genetics, Tohoku University School of Medicine, Sendai, Japan.
  • Kure S; Department of Pediatrics, Tohoku University School of Medicine, Sendai, Japan.
Brain Dev ; 39(4): 337-340, 2017 Apr.
Article en En | MEDLINE | ID: mdl-27916450
We describe the first case of a successful functional hemispherectomy in a patient with epileptic encephalopathy and a de novo collagen type IV alpha 1 (COL4A1) mutation. A 4-year-old girl was COL4A1 mutation-positive and suffered from drug-resistant epilepsy, hemiplegia, and developmental delay. Magnetic resonance imaging detected no porencephaly, and she had no cataract or renal abnormality. Following a presurgical evaluation for epilepsy, she underwent a functional hemispherectomy. She has been seizure free with no intracranial hemorrhage or other perioperative complications. Patients with a COL4A1 mutation have an increased risk for intracranial hemorrhage because of disrupted integrity in the vascular basement membrane due to the mutation. After weighing the risks and benefits to these patients, epilepsy surgery may not be absolutely contraindicated. Furthermore, pediatric neurologists should be aware of an undiagnosed COL4A1 mutation when a patient presents with an unexplained neurological phenotype, such as mild hemiparesis, even in the absence of porencephaly.
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Colágeno Tipo IV / Hemisferectomía / Epilepsia / Mutación Límite: Child, preschool / Female / Humans Idioma: En Revista: Brain Dev Año: 2017 Tipo del documento: Article

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Colágeno Tipo IV / Hemisferectomía / Epilepsia / Mutación Límite: Child, preschool / Female / Humans Idioma: En Revista: Brain Dev Año: 2017 Tipo del documento: Article