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MeSH(Medical Subject Headings) ¸ÂÃã °Ë»ö (http://www.nlm.nih.gov) °á°ú : 5 ÆäÀÌÁö: 3
  • Spinal Dysraphism - »õâ Congenital defects of closure of one or more vertebral arches, which may be associated with malformations of the spinal cord, nerve roots, congenital fibrous bands, lipomas, and congenital cysts. These malformations range from mild (e.g., SPINA BIFIDA OCCULTA) to severe, including rachischisis where there is complete failure of neural tube and spinal cord fusion, resulting in exposure of the spinal cord at the surface. Spinal dysraphism includes all forms of spina bifida. The open form is called SPINA BIFIDA CYSTICA and the closed form is SPINA BIFIDA OCCULTA. (From Joynt, Clinical Neurology, 1992, Ch55, p34)
    Synonyms : Schistorrhachis, Spinal Dysraphia, Bifida, Spina, Dysraphia, Spinal, Dysraphias, Spinal, Dysraphicus, Status, Dysraphism, Spinal, Dysraphisms, Spinal, Rachischises, Spina Bifidas, Spinal Dysraphias, Spinal Dysraphisms
  • Spinal Fractures - »õâ Broken bones in the vertebral column.
    Synonyms : Fracture, Spinal, Fractures, Spinal, Spinal Fracture
  • Spinal Fusion - »õâ Operative immobilization or ankylosis of two or more vertebrae by fusion of the vertebral bodies with a short bone graft or often with diskectomy or laminectomy. (From Blauvelt & Nelson, A Manual of Orthopaedic Terminology, 5th ed, p236; Dorland, 28th ed)
    Synonyms : Fusion, Spinal, Fusions, Spinal, Spinal Fusions, Spondylodeses, Spondylosyndeses
  • Spinal Injuries - »õâ Injuries involving the vertebral column.
    Synonyms : Injuries, Spinal, Injury, Spinal, Spinal Injury
  • Spinal Muscular Atrophies of Childhood - »õâ A group of recessively inherited diseases that feature progressive muscular atrophy and hypotonia. They are classified as type I (Werdnig-Hoffman disease), type II (intermediate form), and type III (Kugelberg-Welander disease). Type I is fatal in infancy, type II has a late infantile onset and is associated with survival into the second or third decade. Type III has its onset in childhood, and is slowly progressive. (J Med Genet 1996 Apr:33(4):281-3)
    Synonyms : HMN (Hereditary Motor Neuropathy) Proximal Type I, Muscular Atrophy, Spinal, Type I, Muscular Atrophy, Spinal, Type II, Muscular Atrophy, Spinal, Type III, Proximal Hereditary Motor Neuropathy Type I, Spinal Muscular Atrophy Type I, Werdnig Hoffman Disease
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MeSH(Medical Subject Headings) À¯»ç °Ë»ö (http://www.nlm.nih.gov) °á°ú : 0 ÆäÀÌÁö: 3
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