| AAPF | anti-arteriosclerosis polysaccharide factor |
|---|---|
| AS | acetylstrophanthidin; acidified serum; acoustic schwannoma; acoustic stimulation; active sarcoidosis... |
| ASO | administrative services only; allele-specific oligonucleoside; antistreptolysin O; arteriosclerosis ... |
| ATS | Achard-Thiers syndrome; acid test solution; alpha-D-tocopherol acid succinate; American Thoracic Soc... |
| GAS | galactorrhea-amenorrhea syndrome; gastric acid secretion; gastrin; gastroenterology; general adaptat... |
| ASO | Arteriosclerosis obliterans |
|---|---|
| EIEE | Early infantile epileptic encephalopathy |
| IHPS | Infantile Hypertrophic Pyloric Stenosis |
| IM | Infantile Myofibromatosis |
| IRD | Infantile Refsum disease |
| arteriosclerosis | <cardiology, disease> Imprecise term for various disorders of arteries, particularly hardening due to fibrosis or calcium deposition, often used as a synonym for atherosclerosis. (17 Oct 1997) |
|---|---|
| arteriosclerosis obliterans | Arteriosclerosis in which proliferation of the intima leads to occlusion of the lumen of the arteries. (12 Dec 1998) |
| medial arteriosclerosis | Arterial sclerosis involving the peripheral arteries, especially of the legs of older people, with deposition of calcium in the medial coat (pipestem arteries) but with little or no encroachment on the lumen. Synonym: medial arteriosclerosis, Monckeberg's calcification, Monckeberg's degeneration, Monckeberg's medial calcification, Monckeberg's sclerosis. (05 Mar 2000) |
| peripheral arteriosclerosis | Arteriosclerosis in any of the vessels beyond the aorta; most often refers to the lower extremities. (05 Mar 2000) |
| Monckeberg's arteriosclerosis | Arterial sclerosis involving the peripheral arteries, especially of the legs of older people, with deposition of calcium in the medial coat (pipestem arteries) but with little or no encroachment on the lumen. Synonym: medial arteriosclerosis, Monckeberg's calcification, Monckeberg's degeneration, Monckeberg's medial calcification, Monckeberg's sclerosis. (05 Mar 2000) |
| coronary arteriosclerosis | Atherosclerosis of the coronary arteries. (12 Dec 1998) |
| senile arteriosclerosis | Arteriosclerosis similar to hypertensive arteriosclerosis, but as a result of advanced age rather than hypertension. (05 Mar 2000) |
| hyperplastic arteriosclerosis | Hyperplasia of the intima and internal elastic layer and hypertrophy of the media independent of atheromatous lesions. (05 Mar 2000) |
| hypertensive arteriosclerosis | Progressive increase in muscle and elastic tissue of arterial walls, resulting from hypertension; in longstanding hypertension, elastic tissue forms numerous concentric layers in the intima and there is replacement of muscle by collagen fibres and hyaline thickening of the intima of arterioles; such changes can develop with increasing age in the absence of hypertension and may then be referred to as senile arteriosclerosis. (05 Mar 2000) |
| nodular arteriosclerosis | Atheromas occurring in the arterial intima as discrete tumours. (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) |
| spasms, infantile | Primary generalised epileptic seizures occurring in infants between birth and twelve months of age consisting of brief synchronous contractions of the neck, torso, and both arms. These seizures often occur in infants with underlying neurologic diseases. The prognosis for these infants is grave, with approximately ninety percent developing mental retardation in addition to their seizures. The eeg has a typical hypsarrhythmia pattern. The spasms and hypsarrhythmia have a tendency to disappear over the first three to five years of life, only to be replaced by other forms of generalised seizures. Infantile spasms sometimes respond to valproic acid or acth. (12 Dec 1998) |
| supravalvar aortic stenosis-infantile hypercalcaemia syndrome | <syndrome> Supravalvar aortic stenosis associated with elfin facies, mental retardation, and hypercalcaemia; usually sporadic; perhaps an irregular dominant trait. (05 Mar 2000) |
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