Diastematomyelia Type 1 with Multiple Spinal Cord and Vertebral Abnormalities in a Child
نویسندگان
چکیده
منابع مشابه
Spinal Cord Analysis in People with Multiple Sclerosis
Background. Multiple Sclerosis (MS) is an autoimmune, inflammatory, and chronic disease which, under the effect of the wastes of myelin degradation occurs in the white matter of the brain, spinal cord, and visual nerves. The main complications of this disease are fatigue, muscle cramps, tremor, imbalance, and walking imbalance. Objectives. The purpose of this study is to investigate the spine ...
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To cite: Gold JJ, Levy ML, Crawford JR. BMJ Case Rep Published online: [please include Day Month Year] doi:10.1136/bcr-2013009799 DESCRIPTION A 12-year-old boy with neurofibromatosis type 1 (NF-1) presented with a giant mass involving the posterior head and neck. The mass was present since 6 months of age and showed considerable growth over the past 2 years that caused extensive disfigurement t...
متن کاملSonographic findings in a neonate with diastematomyelia and a tethered spinal cord.
ongenital midline cutaneous paraspinal lesions, mostly located in the lumbosacral areas, are widely recognized as markers of occult spinal dysraphism. Diastematomyelia, or a split spinal cord, is an unusual congenital spinal abnormality in which the spinal cord is divided into 2 columns by a fibrous, cartilaginous, or bony septum. In most cases, lesions are located on the lower thoracic and upp...
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چکیده ندارد.
Coexistence of multiple rare spinal abnormalities in type 1 neurofibromatosis: a case report and literature review.
Orthopaedic involvement is the most common clinical presentation of Neurofibromatosis type 1 (NF-1) patients with the spinal abnormalities more frequently affected. In the spinal deformities of NF-1 patients, despite the scoliosis is the most frequent finding, several distinctive radiographic features, such as dural ectasia, defective pedicles, and spondylolisthesis, are relatively less common....
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ژورنال
عنوان ژورنال: Clinical Medical Image Library
سال: 2017
ISSN: 2474-3682
DOI: 10.23937/2474-3682/1510067