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Jarcho-Levin syndrome: unusual survival in a classical case.

作者信息

McCall C P, Hudgins L, Cloutier M, Greenstein R M, Cassidy S B

机构信息

Department of Pediatrics, Steele Memorial Children's Research Center, University of Arizona College of Medicine, Tucson.

出版信息

Am J Med Genet. 1994 Feb 1;49(3):328-32. doi: 10.1002/ajmg.1320490317.

Abstract

Spondylothoracic dysostosis, or Jarcho-Levin syndrome, together with spondylocostal dysostosis, constitute a heterogeneous group of rare disorders characterized by short-neck, short-trunk dwarfism and multiple vertebral anomalies at all levels of the vertebral column. The latter include hemivertebrae, fused, hypoplastic, and "butterfly" vertebrae. In most cases of Jarcho-Levin syndrome, the small size of the thorax causes respiratory death in infancy. This report of a Puerto Rican child with spondylothoracic dysostosis and unusually long survival to 11 years exemplifies the nosologic and prognostic difficulties associated with this syndrome.

摘要

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