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Jarcho-Levin syndrome: Report on a long-term follow-up of an untreated patient

  • Tel Aviv University
  • Tel Aviv Sourasky Medical Center
  • Hospital for Special Surgery - New York

Research output: Contribution to journalArticlepeer-review

17 Scopus citations

Abstract

Jarcho-Levin syndrome is a genetically transmitted rare entity characterized by multiple vertebral and rib anomalies. The multilevel skeletal involvement causes short stature, neck and thoracic cage deformities, and restrictive lung disease that is usually the cause of early death. The authors describe a 33-year follow-up of a patient with this syndrome who represents, to their best knowledge, the longest survival of a patient with this entity.

Original languageEnglish
Pages (from-to)150-153
Number of pages4
JournalJournal of Pediatric Orthopaedics Part B
Volume8
Issue number2
DOIs
StatePublished - Apr 1999

Keywords

  • Congenital scoliosis
  • Jarcho-Levin syndrome
  • Spondylocostal dysostosys
  • Spondylothoracic dysostosis

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