Severe scoliosis associated with Costello syndrome: a case report.

T. Motosuneya, T. Asazuma, T. Tsuji, H. Watanabe, Y. Nakayama, K. Nemoto

研究成果: Article

3 引用 (Scopus)

抜粋

Costello syndrome is characterised by dwarfism, unique cutaneous lesions, a distinct facial gestalt, and mental retardation. There have been no detailed reports of severe spinal deformities requiring surgical treatment as a complication of Costello syndrome. We report a case of a 10-year-old girl with progressive scoliosis associated with Costello syndrome. She underwent anterior release and posterior surgical correction and fusion from T5 to L2 using a third generation hook and rod system plus spinous process wiring. Congenital portal vein deficiency and coagulopathy were other major complications. At 15-month follow-up, the patient had good balance and no evidence of instrumentation failure.

元の言語English
ページ(範囲)346-349
ページ数4
ジャーナルJournal of orthopaedic surgery (Hong Kong)
14
発行部数3
DOI
出版物ステータスPublished - 12-2006

All Science Journal Classification (ASJC) codes

  • Surgery

フィンガープリント Severe scoliosis associated with Costello syndrome: a case report.' の研究トピックを掘り下げます。これらはともに一意のフィンガープリントを構成します。

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    Motosuneya, T., Asazuma, T., Tsuji, T., Watanabe, H., Nakayama, Y., & Nemoto, K. (2006). Severe scoliosis associated with Costello syndrome: a case report. Journal of orthopaedic surgery (Hong Kong), 14(3), 346-349. https://doi.org/10.1177/230949900601400324