| PSMA | proximal spinal muscular atrophy |
|---|---|
| PSP | pancreatic spasmolytic peptide; paralytic shellfish poisoning; parathyroid secretory protein; period... |
| SAPF | simultaneous anterior and posterior [spinal] fusion |
| SBMA | spinal bulbar muscular atrophy |
| SCT | secretin; sex chromatin test; sexual compatibility test; sickle-cell trait; sperm cytotoxicity; spin... |
| 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) |
| filum of spinal dura mater | The thread-like termination of the spinal dura mater, surrounding and fused to the filum terminale of the cord, and attached to the deep dorsal sacrococcygeal ligament; extends from S2-3 to Co2 vertebral levels. Synonym: filum durae matris spinalis. (05 Mar 2000) |
| fractional spinal anaesthesia | Insertion of a catheter into the spinal subarachnoid space and leaving it in situ to permit serial intermittent injection of local anaesthetic solution for prolonged spinal anaesthesia. Synonym: fractional spinal anaesthesia. (05 Mar 2000) |
| loops of spinal nerves | Loops of the spinal nerves, connecting ventral primary rami of the spinal nerves. Synonym: ansae nervorum spinalium. (05 Mar 2000) |
| low spinal anaesthesia | Spinal anaesthesia in which the level of sensory denervation extends to the tenth or eleventh thoracic dermatome. (05 Mar 2000) |
| Amberg's lateral sinus line | A line dividing the angle formed by the anterior edge of the mastoid process and the temporal line. (05 Mar 2000) |
| amyotrophic lateral sclerosis | A serious neurologic disease that results from the progressive degeneration of the motor neurons. (27 Sep 1997) |