| SPG | serine phosphoglyceride; spastic paraplegia; splenoportography; sucrose, phosphate, and glutamate; s... |
|---|---|
| SPGX | spastic paraplegia, X-linked |
| ST | esotropia; scala tympani; scaphotrapezoid; sclerotherapy; sedimentation time; semitendinosus; sensor... |
| TSP | testis-specific protein; thrombin-sensitive protein; thrombospondin; total serum protein; total susp... |
| AASP | acute atrophic spinal paralysis; American Association of Senior Physicians; ascending aorta synchron... |
| spastic ectropion | Ectropion of the lower eyelid as a result of ocular irritation. (05 Mar 2000) |
|---|---|
| spastic entropion | Entropion that arises from excessive contracture of the orbicularis oculi muscle. (05 Mar 2000) |
| spastic flat foot | Eversion of the foot with spasm of the muscles (peroneal) on the outer side; often associated with abnormal bars of bone cartilage or fibrous tissue between the calcaneum and the navicular (scaphoid) or between the navicular and the talus, resulting in a tarsal coalition. (05 Mar 2000) |
| spastic gait | Gait in which the leg is stiff, without flexion at knee and ankle, and with each step is rotated away from the body, then towards it, forming a saemicircle. Synonym: circumduction gait, spastic gait. (05 Mar 2000) |
| spastic hemiplegia | A hemiplegia with increased tone in the antigravity muscles of the affected side. (05 Mar 2000) |
| spastic ileus | Intestinal obstruction due to spastic contraction of a segment of the bowel. Synonym: spastic ileus. (05 Mar 2000) |
| spastic mydriasis | Pupillary dilation due to contraction of the dilator muscle of the pupil induced by adrenergic drugs or by stimulation of the sympathetic pathway. (05 Mar 2000) |
| spastic paraplegia | Paresis of the lower extremities with increased muscle tone and spasmodic contraction of the muscles. Synonym: Erb-Charcot disease. (05 Mar 2000) |
| spastic paraplegia, hereditary | An insidiously progressive inherited disorder (probably autosomal dominant) characterised by distal limb weakness. Stiffness of the legs in walking due to the spasticity marks the onset of the disorder. Peripheral sensory neurons may be affected in the later stages of the disease. (12 Dec 1998) |
| spastic pseuodoparalysis | Better known as creutzfeldt-jakob disease (cjd). A dementing disease of the brain. It is believed due to an unconventional (not a bacteria or virus), transmissible agent called a prion. Symptoms of cjd include forgetfulness, nervousness, jerky trembling hand movements, unsteady gait, muscle spasms, chronic dementia, balance disorder, and loss of facial expression. Cjd is classified as a spongiform encephalopathy. most cases occur randomly (sporadically), but inherited forms exist. There is neither treatment nor cure for cjd. Other names for cjd include creutzfeldt-jakob syndrome and jakob-creutzfeldt disease. (12 Dec 1998) |
| spastic speech | Labored speech related to increased tone of muscles. (05 Mar 2000) |
| spastic syndrome in cattle | A disease of the nervous system manifested by spastic contractions of the muscles of one or both hind legs, most common in old bulls; the cramps usually become more frequent and severe, eventually resulting in decreasing the usefulness of the animal. (05 Mar 2000) |
| aggressive infantile fibromatosis | A childhood counterpart of abdominal or extra-abdominal desmoid tumours, characterised by firm subcutaneous nodules that grow rapidly in any part of the body that invade locally and recur but do not metastasize. (05 Mar 2000) |
| autism, infantile | A syndrome beginning in infancy and characterised by a lack of responsiveness to other people, gross impairment in verbal and nonverbal communication skills, and bizarre responses to the environment. (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) |