Literature DB >> 8834041

Multiple vertebral segmentation defects: analysis of 26 new patients and review of the literature.

G R Mortier1, R S Lachman, M Bocian, D L Rimoin.   

Abstract

To further delineate and classify those forms of short trunk dwarfism characterized by multiple vertebral segmentation defects, we analyzed 26 new patients and reviewed 115 described in the literature. Three distinct entities were recognized based on radiographic and clinical findings. Jarcho-Levin syndrome is the lethal autosomal recessive form, characterized by a symmetric crab-like chest. Spondylocostal dysostosis is the benign autosomal dominant condition. Spondylothoracic dysostosis shows considerable clinical and radiographic overlap with spondylocostal dysostosis. Malformations observed in association with multiple vertebral segmentation defects are more common in the sporadic patients. Analysis of the 26 new individuals revealed that the body segment in which these nonvertebral malformations occur corresponds to the site of the vertebral segmentation defects.

Entities:  

Mesh:

Year:  1996        PMID: 8834041     DOI: 10.1002/(SICI)1096-8628(19960202)61:4<310::AID-AJMG3>3.0.CO;2-Y

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  15 in total

1.  Clinical, genetic and environmental factors associated with congenital vertebral malformations.

Authors:  P F Giampietro; C L Raggio; R D Blank; C McCarty; U Broeckel; M A Pickart
Journal:  Mol Syndromol       Date:  2013-02

Review 2.  The mouse notches up another success: understanding the causes of human vertebral malformation.

Authors:  Duncan B Sparrow; Gavin Chapman; Sally L Dunwoodie
Journal:  Mamm Genome       Date:  2011-06-11       Impact factor: 2.957

3.  A gene for autosomal recessive spondylocostal dysostosis maps to 19q13.1-q13.3.

Authors:  P D Turnpenny; M P Bulman; T M Frayling; T K Abu-Nasra; C Garrett; A T Hattersley; S Ellard
Journal:  Am J Hum Genet       Date:  1999-07       Impact factor: 11.025

Review 4.  Congenital and idiopathic scoliosis: clinical and genetic aspects.

Authors:  Philip F Giampietro; Robert D Blank; Cathleen L Raggio; Sajid Merchant; F Stig Jacobsen; Thomas Faciszewski; Sanjay K Shukla; Anne R Greenlee; Cory Reynolds; David B Schowalter
Journal:  Clin Med Res       Date:  2003-04

5.  Chromosome 18q22.2-->qter deletion and a congenital anomaly syndrome with multiple vertebral segmentation defects.

Authors:  S B Dowton; A V Hing; V Sheen-Kaniecki; M S Watson
Journal:  J Med Genet       Date:  1997-05       Impact factor: 6.318

6.  A retrospective study of congenital scoliosis and associated cardiac and intraspinal abnormities in a Chinese population.

Authors:  Yong-tai Liu; Li-lin Guo; Zhuang Tian; Wen-ling Zhu; Bin Yu; Shu-yang Zhang; Gui-xing Qiu
Journal:  Eur Spine J       Date:  2011-05-01       Impact factor: 3.134

7.  Tomographic assessment of the spine in children with spondylocostal dysotosis syndrome.

Authors:  Ali Al Kaissi; Klaus Klaushofer; Franz Grill
Journal:  Clinics (Sao Paulo)       Date:  2010       Impact factor: 2.365

8.  Novel mutations in DLL3, a somitogenesis gene encoding a ligand for the Notch signalling pathway, cause a consistent pattern of abnormal vertebral segmentation in spondylocostal dysostosis.

Authors:  P D Turnpenny; N Whittock; J Duncan; S Dunwoodie; K Kusumi; S Ellard
Journal:  J Med Genet       Date:  2003-05       Impact factor: 6.318

9.  Jarcho-Levin syndrome.

Authors:  M L Kulkarni; Sarfaraz R Navaz; H N Vani; K S Manjunath; Deepa Matani
Journal:  Indian J Pediatr       Date:  2006-03       Impact factor: 5.319

10.  Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy in an Israeli family.

Authors:  Radi Shahien; Silvia Bianchi; Abdalla Bowirrat
Journal:  Neuropsychiatr Dis Treat       Date:  2011-06-20       Impact factor: 2.570

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