Foramen Magnum Decompression for Chiari Malformation Type Ⅰ Complicated by Craniometaphyseal Dysplasia : A Case Report and Literature Review
Author:
Affiliation:
1. Department of Neurosurgery, Nagoya University Hospital
2. Department of Neurosurgery, Japanese Red Cross Nagoya Daiichi Hospital
Publisher
The Japanese Congress of Neurological Surgeons
Subject
Neurology (clinical),Surgery
Link
https://www.jstage.jst.go.jp/article/jcns/30/7/30_539/_pdf
Reference17 articles.
1. 1) Beiphton P : Craniometaphyseal dysplasia (CMD), autosomal dominant form. J Med Genet 32 : 370-374, 1995.
2. 2) Cai C, Zhang Q, Shen C, Sun G, Wang C : Chiari malformation caused by craniometaphyseal dysplasia : case report and review of literature. Eur J Pediatr Surg 18 : 198-201, 2008.
3. 3) Chen IP, Wang L, Jiang X, Aguila HL, Reichenberger EJ : A Phe377del mutation in ANK leads to impaired osteoblastogenesis and osteoclastogenesis in a mouse model for craniometaphyseal dysplasia (CMD). Hum Mol Genet 20 : 948-961, 2011.
4. 4) Day RA, Park TS, Ojemann JG, Kaufman BA : Foramen magnum decompression for cervicomedullary encroachment in craniometaphyseal dysplasia : case report. Neurosurgery 41 : 960-964, 1997.
5. 5) Frantz DC, Horn KL, Aase J : Craniometaphyseal dysplasia : operative findings and treatment. Am J Otol 17 : 283-287, 1996.
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