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Published in: Indian Journal of Pediatrics 6/2018

01-06-2018 | Picture of the Month

Spondylocostal Dysostosis (Jarcho Levin Syndrome)

Authors: Praveen M. Kurup, Vasanthan Tanigasalam, B. Vishnu Bhat

Published in: Indian Journal of Pediatrics | Issue 6/2018

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Excerpt

A term female neonate with a birth weight of 3.25 kg was tachypneic at birth. The neonate had a short neck, scoliosis to the right side of the chest and asymmetric chest wall with heart sounds heard on the right side of the chest (Fig. 1). The neonate’s rib cage was deficient on the left side with a soft tissue swelling moving with respiration. It was suggestive of lung herniation. Chest skiagram showed congenital absence of left 6th and 7th ribs, partial fusion of left 8th and 9th ribs, partial fusion of right 5th, 6th and 7th ribs, scoliosis of the spine to the right side of chest and hemivertebra (Fig. 2). The echocardiography was normal. These features were consistent with the diagnosis of Spondylocostal dysostosis or Jarcho-Levin syndrome.
Literature
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go back to reference Chandra N, Kumar S, Raj V, Vishwakarma PK, Sinha S, Saha RP. Jarcho-Levin syndrome with splenic herniation: a rare presentation. Am J Case Rep. 2016;17:745–8.CrossRefPubMedPubMedCentral Chandra N, Kumar S, Raj V, Vishwakarma PK, Sinha S, Saha RP. Jarcho-Levin syndrome with splenic herniation: a rare presentation. Am J Case Rep. 2016;17:745–8.CrossRefPubMedPubMedCentral
2.
go back to reference Beine O, Bolland J, Verloes A, Lebrun FR, Khamis J, Muller C. Spondylocostal dysostosis: a rare genetic disease. Rev Med Liege. 2004;59:513–6.PubMed Beine O, Bolland J, Verloes A, Lebrun FR, Khamis J, Muller C. Spondylocostal dysostosis: a rare genetic disease. Rev Med Liege. 2004;59:513–6.PubMed
Metadata
Title
Spondylocostal Dysostosis (Jarcho Levin Syndrome)
Authors
Praveen M. Kurup
Vasanthan Tanigasalam
B. Vishnu Bhat
Publication date
01-06-2018
Publisher
Springer India
Published in
Indian Journal of Pediatrics / Issue 6/2018
Print ISSN: 0019-5456
Electronic ISSN: 0973-7693
DOI
https://doi.org/10.1007/s12098-017-2549-0

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