| ALH | angiolymphoid hyperplasia; anterior lobe hormone; anterior lobe of hypophysis |
|---|---|
| APL | abductor pollicis longus; accelerated painless labor; acute promyelocytic leukemia; animal placenta ... |
| CA | anterior commissure [Lat. commissura anterior]; calcium antagonist; California [rabbit]; cancer; Can... |
| LADA | laboratory animal dander allergy; left acromio-dorso-anterior [position]; left anterior descending a... |
| OA | obstructive apnea; occipital artery; occipito-anterior; occiput anterior; octanoic acid; ocular albi... |
| muscular atrophy, spinal | Progressive degenerative disorder of motor neurons in the spinal cord, brainstem, and motor cortex, manifested clinically by muscular weakness, atrophy, and corticospinal tract signs in varying combinations. (12 Dec 1998) |
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| continuous 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) |
| posterior branch of spinal nerves | See: dorsal primary ramus of spinal nerve. (05 Mar 2000) |
| posterior spinal artery | <anatomy, artery> Origin, vertebral; distribution, medulla, spinal cord, and pia mater; anastomoses, spinal branches of intercostal arteries. Synonym: arteria spinalis posterior. (05 Mar 2000) |
| posterior spinal sclerosis | See Tabes dorsalis. (12 Dec 1998) |
| progressive 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) |
| progressive spinal amyotrophy | A serious neurologic disease that results from the progressive degeneration of the motor neurons. (27 Sep 1997) |
| progressive spinal muscular atrophy | One of the subgroups of motor neuron disease; a progressive degenerative disorder of the motor neurons of the spinal cord, manifested as progressive, often symmetrical, weakness and wasting, typically beginning in the distal portions of the limbs, particularly in the upper extremities, and spreading proximally; fasciculation potentials are often present, but evidence of corticospinal tract disease (e.g., increased deep tendon reflexes, Babinski sign) is not. (05 Mar 2000) |
| hereditary spinal ataxia | Sclerosis of the posterior and lateral columns of the spinal cord, occurring in children and marked by ataxia in the lower extremities, extending to the upper, followed by paralysis and contractures; autosomal recessive inheritance. See: spinocerebellar ataxia. Synonym: Friedreich's ataxia, heredotaxia. (05 Mar 2000) |
| high spinal anaesthesia | Spinal anaesthesia in which the level of sensory denervation extends to the second or third thoracic dermatome. (05 Mar 2000) |
| hyperbaric spinal anaesthesia | Spinal anaesthesia in which spread of local anaesthetic solution in the subarachnoid space is controlled by adjusting the position of the patient when the density of local anaesthetic is made greater than the density of cerebrospinal fluid (i.e., hyperbaric) by the addition of glucose. (05 Mar 2000) |
| hypobaric spinal anaesthesia | <anaesthetics> Spinal anaesthesia in which spread of local anaesthetic solution in the subarachnoid space is controlled by adjusting the position of the patient when the density of the local anaesthetic solution is made less than the density of cerebrospinal fluid (i.e., hypobaric) by the addition of distilled water. (05 Mar 2000) |
| hysterical spinal neuralgia | Simulating Pott's disease, following a trauma. (05 Mar 2000) |
| spastic spinal paralysis | A type of cerebral palsy in which there is bilateral spasticity, with the lower extremities more severely affected. Compare: flaccid paralysis. Synonym: Erb-Charcot disease, infantile diplegia, Little's disease, spastic spinal paralysis, tabes spasmodica. (05 Mar 2000) |
| spinal | <anatomy> Pertaining to a spine or to the vertebral column. Origin: L. Spinalis (18 Nov 1997) |