| ARSACS | autosomal recessive spastic ataxia of Charlevoix-Saguenay |
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| FSP | familial spastic paraplegia; fibrin split products; fibrinogen split products; fine suspended partic... |
| HSP | Health Systems Plan; heat shock protein; hemostatic screening profile; Henoch-Schonlein purpura; her... |
| SPERM | spastic paraplegia-epilepsy-mental retardation [syndrome] |
| SPG | serine phosphoglyceride; spastic paraplegia; splenoportography; sucrose, phosphate, and glutamate; s... |
| paraparesis, tropical spastic | Subacute paralytic myeloneuropathy occurring endemically in tropical areas such as the caribbean, colombia, india, and africa, as well as in the southwestern region of japan; associated with infection by type I human lymphotropic retrovirus (HTLV-I). Toxic nutritional factors have largely been ruled out as the cause of this syndrome, the primary clinical feature of which is progressive weakness of the legs and lower body. (12 Dec 1998) |
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| colitis, spastic | See Colitis, mucus. (12 Dec 1998) |
| congenital spastic paraplegia | A spastic paralysis of the lower extremities occurring in the infant. Synonym: infantile spastic paraplegia. (05 Mar 2000) |
| pseuodoparalysis, spastic | Better known as creutzfeldt-jakob disease. 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 | 1. Of the nature of or characterised by spasms. 2. Hypertonic, so that the muscles are stiff and the movements awkward. 3. A person exhibiting spasticity, such as occurs in spastic paralysis or in cerebral palsy. Origin: Gr. Spastikos (13 Nov 1997) |
| spastic abasia | Abasia due to a spastic contraction of the muscles when an attempt is made to walk. (05 Mar 2000) |
| spastic anaemia | Local anaemia resulting from nontransitory contraction of the arterial vessels in the affected region. (05 Mar 2000) |
| spastic colitis | See Syndrome, irritable bowel. (12 Dec 1998) |
| spastic colon | A bowel disorder with no demonstrable organic abnormality. Often referred to as a functional bowel disorder or spastic colon. Symptoms include episodic, crampy abdominal pains often related to anxiety. (27 Sep 1997) |
| spastic diplegia | 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) |
| spastic dysarthria | Dysarthria caused by lesions along the corticobulbar tracts. Synonym: rigid dysarthria. (05 Mar 2000) |
| spastic dysphonia | A spasmodic contraction of the intrinsic muscles of the larynx excited by attempted phonation, producing either adductor or abductor subtypes caused by central nervous system disease. A localised form of movement disorder. Synonym: phonic spasm, spastic dysphonia. (05 Mar 2000) |
| 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 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) |