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العنوان
Prognosis of Spina Bifida Cystica /
المؤلف
Kenawy, Karam Kenawy Gad Allah.
هيئة الاعداد
باحث / كرم قناوى جاد الله قناوى
مشرف / رشدى عبد العزيز الخياط
مناقش / محمد احمد عبدالعال
مناقش / احمد ابراهيم الغريانى
الموضوع
Neurosurgery.
تاريخ النشر
2008.
عدد الصفحات
111 P. ;
اللغة
الإنجليزية
الدرجة
ماجستير
التخصص
جراحة
الناشر
تاريخ الإجازة
27/12/2010
مكان الإجازة
جامعة أسيوط - كلية الطب - Neuroscience
الفهرس
Only 14 pages are availabe for public view

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from 124

Abstract

Neural tube defects are group of congenital anomalies characterized by defects in dorsal midline structures, including neural tissue, dura, muscle, bone and/or skin. Spinal dysraphism refer to those anomalies affecting bony and/or nervous components of the spine. The primary embryological defect is believed to be a failure of, or incomplete, neural tube closure. This is a process that normally occurs during the third to fourth week of fetal life .
These lesions can involve any part of the spine, although they most often involve the lumbosacral spine, and range from a simple gap in the lamina of a single vertebral level to an extensive dorsal opening with an exposed spinal cord. The incidence of spinal dysraphism is estimated at 0.05 to 0.25 per 1000 live births per year and increased in developing countries .
Severe spinal dysraphic disorders constitute a major source of disability among children and adults. Management of spinal dysraphic anomalies involves a number of steps: accurate diagnosis; an assessment of the severity of the lesion; a decision whether intervention is warranted; the nature of the intervention; and educating the family of the need for lifelong medical care.