Spinal and pelvic corrections in a patient with spondylocostal dysplasia syndrome and hemimyelomeningocele
Standard
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/Zeitung › SCORING: Zeitschriftenaufsatz › Forschung › Begutachtung
Harvard
APA
Vancouver
Bibtex
}
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 -