Literature DB >> 23605835

Sprengel's deformity: association with musculoskeletal dysfunctions and tethered cord syndrome.

Nimish Mittal1, Ritu Majumdar, Sonal Chauhan, Minati Acharjya.   

Abstract

Sprengel's deformity is a rare and complex congenital deformity of the shoulder girdle. The deformity commonly occurs sporadically, though in combination with other congenital anomalies, such as congenital scoliosis, fusion of cervical vertebrae, and conditions like Klippel-Feil syndrome may coexist. We report a case of a 14-year-old girl with bilateral Sprengel's deformity presenting with a progressive bilateral lower limb weakness and gait abnormality. Radiological investigations demonstrated multiple musculoskeletal abnormalities on x-ray and lumbar spina bifida occulta causing tethering of the cord on MRI. The patient consulted neurosurgeons and orthopaedic surgeons, who recommended no operative intervention and conservative management till the end of growth spurt. Therefore, we prescribed a home-based exercise regimen to strengthen the periscapular and intrinsic foot muscles. Although rare, Sprengel's deformity can be associated with other musculoskeletal abnormalities including lumbar spina bifida and comprehensive neurological examination should not be ignored as it is much more than a cosmetic problem.

Entities:  

Mesh:

Year:  2013        PMID: 23605835      PMCID: PMC3645234          DOI: 10.1136/bcr-2013-009182

Source DB:  PubMed          Journal:  BMJ Case Rep        ISSN: 1757-790X


  7 in total

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Journal:  Can Med Assoc J       Date:  1934-12       Impact factor: 8.262

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Journal:  J Bone Joint Surg Am       Date:  1981-10       Impact factor: 5.284

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Journal:  J Bone Joint Surg Br       Date:  1983-11

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  7 in total
  2 in total

1.  Cord injury after spinal anaesthesia in a patient with previously undiagnosed Klippel-Feil syndrome.

Authors:  E Stevens; B Williams; N Kock; M Kitching; M P Simpson
Journal:  Anaesth Rep       Date:  2019-03-11

2.  The VANGL1 P384R variant cause both neural tube defect and Klippel-Feil syndrome.

Authors:  Chen Cheng; Sheng Zhao; Xia Zhu; Fan Yang; Weiyun Wang; Qian Feng; Ya Liu; Hui Huang; Xinlin Chen
Journal:  Mol Genet Genomic Med       Date:  2021-05-20       Impact factor: 2.183

  2 in total

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