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Spondylocostal dysostosis with lipomyelomeningocele: Case report and review of the literature

Spondylocostal dysostosis (SCDO) is rare anomaly caused due to flawed embryological development of the axial skeleton during preliminary stages of gravidity, characterized by malformed vertebral column and ribs, abridged thorax and kyphoscoliosis. This entity was also reported as a “Jarcho–Levin syn...

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Autores principales: Anjankar, Shailendra D., Subodh, Raju
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4302546/
https://www.ncbi.nlm.nih.gov/pubmed/25624929
http://dx.doi.org/10.4103/1817-1745.147580
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author Anjankar, Shailendra D.
Subodh, Raju
author_facet Anjankar, Shailendra D.
Subodh, Raju
author_sort Anjankar, Shailendra D.
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description Spondylocostal dysostosis (SCDO) is rare anomaly caused due to flawed embryological development of the axial skeleton during preliminary stages of gravidity, characterized by malformed vertebral column and ribs, abridged thorax and kyphoscoliosis. This entity was also reported as a “Jarcho–Levin syndrome” eponym by erstwhile authors, before the introduction of genetic based classification. A literature review showed only three cases of this clinical entity with lipomyelomeningocele. We report the fourth case report of an infant with SCDO with lipomyelomeningocele. His chest X-ray displayed absent left side 6(th)–8(th) ribs with peculiar fan like configuration, making the heart vulnerable to any direct injury. Special care has to be taken for such patients who need surgical procedure in the prone position.
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spelling pubmed-43025462015-01-26 Spondylocostal dysostosis with lipomyelomeningocele: Case report and review of the literature Anjankar, Shailendra D. Subodh, Raju J Pediatr Neurosci Case Report Spondylocostal dysostosis (SCDO) is rare anomaly caused due to flawed embryological development of the axial skeleton during preliminary stages of gravidity, characterized by malformed vertebral column and ribs, abridged thorax and kyphoscoliosis. This entity was also reported as a “Jarcho–Levin syndrome” eponym by erstwhile authors, before the introduction of genetic based classification. A literature review showed only three cases of this clinical entity with lipomyelomeningocele. We report the fourth case report of an infant with SCDO with lipomyelomeningocele. His chest X-ray displayed absent left side 6(th)–8(th) ribs with peculiar fan like configuration, making the heart vulnerable to any direct injury. Special care has to be taken for such patients who need surgical procedure in the prone position. Medknow Publications & Media Pvt Ltd 2014 /pmc/articles/PMC4302546/ /pubmed/25624929 http://dx.doi.org/10.4103/1817-1745.147580 Text en Copyright: © Journal of Pediatric Neurosciences http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Anjankar, Shailendra D.
Subodh, Raju
Spondylocostal dysostosis with lipomyelomeningocele: Case report and review of the literature
title Spondylocostal dysostosis with lipomyelomeningocele: Case report and review of the literature
title_full Spondylocostal dysostosis with lipomyelomeningocele: Case report and review of the literature
title_fullStr Spondylocostal dysostosis with lipomyelomeningocele: Case report and review of the literature
title_full_unstemmed Spondylocostal dysostosis with lipomyelomeningocele: Case report and review of the literature
title_short Spondylocostal dysostosis with lipomyelomeningocele: Case report and review of the literature
title_sort spondylocostal dysostosis with lipomyelomeningocele: case report and review of the literature
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4302546/
https://www.ncbi.nlm.nih.gov/pubmed/25624929
http://dx.doi.org/10.4103/1817-1745.147580
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