Spinal and pelvic corrections in a patient with spondylocostal dysplasia syndrome and hemimyelomeningocele

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Spinal and pelvic corrections in a patient with spondylocostal dysplasia syndrome and hemimyelomeningocele. / Al Kaissi, Ali; Stücker, Ralf; Ganger, Rudolf; Klaushofer, Klaus; Grill, Franz.

in: Afr J Paediatr Surg, Jahrgang 11, Nr. 4, 2014, S. 341-346.

Publikationen: SCORING: Beitrag in Fachzeitschrift/ZeitungSCORING: ZeitschriftenaufsatzForschungBegutachtung

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@article{55843361f4044959adc611f79feb9209,
title = "Spinal and pelvic corrections in a patient with spondylocostal dysplasia syndrome and hemimyelomeningocele",
abstract = "Congenital malformation complex of the spine and the spinal cord can be a syndromic entity rather than a symptom complex. The spinal cord lesion is usually bilaterally symmetrical, but, there are occasional cases with one or more hemivertebrae, often associated with a central bony spur splitting the cord (diastematomyelia), in which one leg is virtually normal while the other is severely paralysed. Hemimyelomeningocele over the lumbar area may be associated with extensive spine malsegmentation compatible with the diagnosis of spondylocostal dysplasia syndrome. In this report, we present a 3-year-old girl who underwent neurological evaluation and spinal imaging studies for extensive spine malsegmentation compatible with spondylocostal dysostosis syndrome associated with hemimyelomeningocele. She had a series of corrective orthopaedic interventions to reconstruct her pelvic girdle and spine deformities, with a satisfactory outcome.",
author = "{Al Kaissi}, Ali and Ralf St{\"u}cker and Rudolf Ganger and Klaus Klaushofer and Franz Grill",
year = "2014",
doi = "10.4103/0189-6725.143163",
language = "English",
volume = "11",
pages = "341--346",
journal = "Afr J Paediatr Surg",
issn = "0189-6725",
publisher = "Medknow Publications and Media Pvt. Ltd",
number = "4",

}

RIS

TY - JOUR

T1 - Spinal and pelvic corrections in a patient with spondylocostal dysplasia syndrome and hemimyelomeningocele

AU - Al Kaissi, Ali

AU - Stücker, Ralf

AU - Ganger, Rudolf

AU - Klaushofer, Klaus

AU - Grill, Franz

PY - 2014

Y1 - 2014

N2 - Congenital malformation complex of the spine and the spinal cord can be a syndromic entity rather than a symptom complex. The spinal cord lesion is usually bilaterally symmetrical, but, there are occasional cases with one or more hemivertebrae, often associated with a central bony spur splitting the cord (diastematomyelia), in which one leg is virtually normal while the other is severely paralysed. Hemimyelomeningocele over the lumbar area may be associated with extensive spine malsegmentation compatible with the diagnosis of spondylocostal dysplasia syndrome. In this report, we present a 3-year-old girl who underwent neurological evaluation and spinal imaging studies for extensive spine malsegmentation compatible with spondylocostal dysostosis syndrome associated with hemimyelomeningocele. She had a series of corrective orthopaedic interventions to reconstruct her pelvic girdle and spine deformities, with a satisfactory outcome.

AB - Congenital malformation complex of the spine and the spinal cord can be a syndromic entity rather than a symptom complex. The spinal cord lesion is usually bilaterally symmetrical, but, there are occasional cases with one or more hemivertebrae, often associated with a central bony spur splitting the cord (diastematomyelia), in which one leg is virtually normal while the other is severely paralysed. Hemimyelomeningocele over the lumbar area may be associated with extensive spine malsegmentation compatible with the diagnosis of spondylocostal dysplasia syndrome. In this report, we present a 3-year-old girl who underwent neurological evaluation and spinal imaging studies for extensive spine malsegmentation compatible with spondylocostal dysostosis syndrome associated with hemimyelomeningocele. She had a series of corrective orthopaedic interventions to reconstruct her pelvic girdle and spine deformities, with a satisfactory outcome.

U2 - 10.4103/0189-6725.143163

DO - 10.4103/0189-6725.143163

M3 - SCORING: Journal article

C2 - 25323186

VL - 11

SP - 341

EP - 346

JO - Afr J Paediatr Surg

JF - Afr J Paediatr Surg

SN - 0189-6725

IS - 4

ER -