2015, Volume 8, Issue 3, pp 388 – 397

Congenital scoliosis: an up-to-date

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Authors and Affiliations

Correspondence to: Prof. Gheorghe Burnei, MD “Maria Sklodowska Curie” Clinical Emergency Hospital for Children, 20 C-tin Brancoveanu Street, Bucharest, Romania Mobile phone: +40755 110 100, E-mail: mscburnei@yahoo.com

Abstract

Congenital scoliosis represents a spinal malformation due to defects of formation, segmentation or mixed ones. It is characterized by a longitudinal and rotational imbalance.

54 patients were analyzed and 39 out of them were operated by various approaches with anterior and posterior instrumentations during 2000 and 2012. The impossibility to appoint some patients encountered in the daily practice into the known classifications, allowed us to purpose two categories of congenital scoliosis related to the predominance of spinal deviances in the coronal and transversal views.

No certain etiology of congenital scoliosis has been identified until today. The susceptibility of some polygenic defects is obvious due to the presence of a sum of defects associated to most of the congenital scoliosis cases and the rarity of the presence of a unique defect.

The diagnosis requires a thorough clinical and imaging examination in order to establish an individualized therapeutic strategy.

The treatment of congenital scoliosis is different from the adolescent idiopathic one. Therapeutic criteria are significantly different. It is essential to assess the difference in growth of the concavity related to the convexity when choosing a particular procedure. The magnitude of the curve and the progressive rate are fundamental issues to the surgeon

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About this article

PMC ID: 4556925
PubMed ID: 26351546
DOI: 

Article Publishing Date (print): Jul-Sep 2015
Available Online: 

Journal information

ISSN Printing: 1844-122X
ISSN Online: 1844-3117
Journal Title: Journal of Medicine and Life

Copyright License: Open Access

This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use and redistribution provided that the original author and source are credited.


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