| dura mater of spinal cord | Single-layered strong membrane, comparable to and continuous with (at foramen magnum) the meningeal layer of the intracranial dura mater of the brain. It does not (in contrast to the dura mater of brain) adhere to the enveloping bony structures (vertebrae) or their periosteum, being separated from the latter by a considerable space, the vertebral epidural space-a true space containing the internal vertebral venous plexus embedded in a matrix of epidural fat. Synonym: dura mater spinalis, endorrhachis, theca vertebralis. (05 Mar 2000) |
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| infantile progressive spinal muscular atrophy | Transmitted as autosomal recessive on chromosome 5q. Progressive dysfunction of the anterior horn cells in the spinal cord and brainstem cranial nerves with profound weakness and bulbar dysfunction occurring in the first two years of life. Three groups, based on age of clinical onset, are recognised. Synonym: familial spinal muscular atrophy, Hoffmann's muscular atrophy, infantile muscular atrophy, infantile progressive spinal muscular atrophy, progressive infantile spinal muscular atrophy, Werdnig-Hoffmann disease, Werdnig-Hoffmann muscular atrophy. (05 Mar 2000) |
| infantile spinal muscular atrophy | Transmitted as autosomal recessive on chromosome 5q. Progressive dysfunction of the anterior horn cells in the spinal cord and brainstem cranial nerves with profound weakness and bulbar dysfunction occurring in the first two years of life. Three groups, based on age of clinical onset, are recognised. Synonym: familial spinal muscular atrophy, Hoffmann's muscular atrophy, infantile muscular atrophy, infantile progressive spinal muscular atrophy, progressive infantile spinal muscular atrophy, Werdnig-Hoffmann disease, Werdnig-Hoffmann muscular atrophy. (05 Mar 2000) |
| intermediolateral cell column of spinal cord | The cell column that forms the lateral horn of the spinal cord's gray matter. Extending from the first thoracic through the second lumbar segment, the column contains the autonomic motor neurons that give rise to the preganglionic fibres of the sympathetic system. Synonym: intermediolateral cell column of spinal cord, nucleus intermediolateralis. (05 Mar 2000) |
| isobaric spinal anaesthesia | Spinal anaesthesia of same density as cerobrospinal fluid so that the level of anaesthesia is not influenced by a change in the position of the patient. (05 Mar 2000) |
| thoracic part of spinal cord | The part of the spinal cord which consists of the twelve thoracic segments of the spinal cord from which the twelve pairs of thoracic nerves originate. Synonym: pars thoracica medullae spinalis, segmenta medullae spinalis thoracica. (05 Mar 2000) |
| thoracic spinal nerves | Twelve nerves on each side, mixed motor and sensory, supplying the muscles and skin of the thoracic and abdominal walls. Synonym: nervi thoracici. (05 Mar 2000) |
| total spinal anaesthesia | Spinal anaesthesia extensive enough to produce loss of sensation in all extracranial sensory roots. (05 Mar 2000) |
| trigeminal nucleus, spinal | Nucleus of the spinal tract of the trigeminal nerve. It is divided cytoarchitectonically into three parts: oralis, caudalis (trigeminal caudal nucleus), and interpolaris. (12 Dec 1998) |
| equine spinal ataxia | A disease of young horses characterised by progressive weakness and incoordination, most evident in the hind legs; it is associated with lesions in the cervical region of the spinal cord and is the result of compression of the spinal cord by malformed cervical vertebrae. (05 Mar 2000) |
| Erb spinal paralysis | Chronic myelitis of syphilitic origin. (05 Mar 2000) |
| erector-spinal reflex | A contraction of part of the erector spinae muscle following scratching of the skin on its outer border. (05 Mar 2000) |
| tuberculosis, spinal | Osteitis or caries of the vertebrae, usually occurring as a complication of tuberculosis of the lungs. (12 Dec 1998) |
| juvenile spinal muscular atrophy | Slowly progressive proximal muscular weakness and wasting, beginning in childhood, caused by degeneration of motor neurons in the anterior horns of the spinal cord; onset usually between 2 and 17 years of age; usually autosomal recessive inheritance. Synonym: juvenile muscular atrophy, Kugelberg-Welander disease, Wohlfart-Kugelberg-Welander disease. (05 Mar 2000) |
| familial spinal muscular atrophy | Transmitted as autosomal recessive on chromosome 5q. Progressive dysfunction of the anterior horn cells in the spinal cord and brainstem cranial nerves with profound weakness and bulbar dysfunction occurring in the first two years of life. Three groups, based on age of clinical onset, are recognised. Synonym: familial spinal muscular atrophy, Hoffmann's muscular atrophy, infantile muscular atrophy, infantile progressive spinal muscular atrophy, progressive infantile spinal muscular atrophy, Werdnig-Hoffmann disease, Werdnig-Hoffmann muscular atrophy. (05 Mar 2000) |