A Patient with a Type I Split Cord Malformation and an Open Myelomeningocele without Advanced Lower Limb Paresis: A Case Report and a Review of the Literature
Author:
Affiliation:
1. Department of Neurosurgery, Yamagata University, Faculty of Medicine, Yamagata, Yamagata, Japan
Publisher
Japan Neurosurgical Society
Subject
Polymers and Plastics,General Environmental Science
Link
https://www.jstage.jst.go.jp/article/nmccrj/8/1/8_cr.2020-0037/_pdf
Reference12 articles.
1. 1) Pang D, Dias MS, Ahab-Barmada M: Split cord malformation: Part I: A unified theory of embryogenesis for double spinal cord malformations. Neurosurgery 31: 451–480, 1992
2. 2) Pang D: Split cord malformation: Part II: clinical syndrome. Neurosurgery 31: 481–500, 1992
3. 3) Pang D: 34 split cord malformation: from gastrulation to operation, in Cohen AR: Pediatric Neurosurgery: Tricks of the Trade, New York, Thieme, 2016, pp. 293–305
4. 4) Rowley VB, Johnson AJ: Lumbar split cord malformation with lateral hemimyelomeningocele and associated Chiari II malformation and other visceral and osseous anomalies: a case report. J Comput Assist Tomogr 33: 923–926, 2009
5. 5) Yamanaka T, Hashimoto N, Sasajima H, Mineura K: A case of diastematomyelia associated with myeloschisis in a hemicord. Pediatr Neurosurg 35: 253–256, 2001
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