Literature DB >> 6450976

[Diastematomelia (author's transl)].

B Lassale, P Rigault, J C Pouliquen, J P Padovani, G Guyonvarch.   

Abstract

21 cases have been observed and followed up for 10 years. All were children. Three types of anomaly were noted: Spinal curvature (mostly scoliosis), skin abnormalities in the mid line (hypertrichosis, angioma, skin dimples) and problems in the lower limbs (varus deformities of the feet, leg length discrepancy, muscular atrophy, neurological disorders). These signs, even if not all are present, must lead to a study of the vertebral bodies and to gas myelography whcih demonstrates a double spinal cord over a variable length from 2 to 14 segments. 15 children were treated surgically by mobilisation of the spinal cord and arthrodesis of the spine. 4 of them were made worse. In contrast, none of the 6 children treated conservately was made worse. The authors conclude that surgery should be reserved for recent spontaneous neurological deterioration and severe deformities of the spine.

Entities:  

Mesh:

Year:  1980        PMID: 6450976

Source DB:  PubMed          Journal:  Rev Chir Orthop Reparatrice Appar Mot        ISSN: 0035-1040


  3 in total

Review 1.  Split spinal cord malformations: report of 22 cases and review of the literature.

Authors:  Edgardo Schijman
Journal:  Childs Nerv Syst       Date:  2003-02-05       Impact factor: 1.475

2.  The operative treatment of congenital scoliosis. A review of 26 cases.

Authors:  P Griss; H Huberti
Journal:  Arch Orthop Trauma Surg       Date:  1981

Review 3.  Split cord malformation and tethered cord syndrome: case series with long-term follow-up and literature review.

Authors:  Andrew J Kobets; Jeffrey Oliver; Alan Cohen; George I Jallo; Mari L Groves
Journal:  Childs Nerv Syst       Date:  2020-11-26       Impact factor: 1.475

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.