| acc | insuff accommodation insufficiency |
|---|---|
| AMVI | acute mesenteric vascular insufficiency |
| BAI | basilar artery insufficiency; beta-aminoisobutyrate |
| card | insuff cardiac insufficiency |
| CCI | Cardiovascular Credentialing International; cholesterol crystallization inhibitor; chronic coronary ... |
| divergence insufficiency | That condition in which an exophoria or exotropia is more marked for near vision than for far vision. (05 Mar 2000) |
|---|---|
| divergence insufficiency exotropia | Exotropia in which the strabismus is notably greater for near vision than for far vision. (05 Mar 2000) |
| insufficiency | The condition of being insufficient or inadequate to the performance of the allotted duty. Origin: L. Insufficientia, from sufficiens = sufficient (18 Nov 1997) |
| thyroid insufficiency | Subnormal secretion of hormones by the thyroid gland. See: hypothyroidism. (05 Mar 2000) |
| tricuspid insufficiency | See: valvular insufficiency. (05 Mar 2000) |
| tricuspid valve insufficiency | Backflow of blood from the right ventricle into the right atrium, owing to imperfect functioning of the tricuspid valve. (12 Dec 1998) |
| exocrine pancreatic insufficiency | Lack of exocrine secretions of pancreas, due to destruction of acini, usually by chronic pancreatitis; lack of digestive enzymes from pancreas results in diarrhoea, usually fatty (steatorrhoea) because of lack of pancreatic enzymes. (05 Mar 2000) |
| uterine insufficiency | Atony of the uterine musculature. (05 Mar 2000) |
| latent adrenocortical insufficiency | Adrenocortical insufficiency not clinically evident but which can become severe if a sudden stress, such as an intercurrent acute illness, develops. (05 Mar 2000) |
| adult pseudohypertrophic muscular dystrophy | Muscular dystrophy of late onset, often in the second or third decade, with relatively mild course; X-linked recessive inheritance; perhaps allelic with Duchenne's dystrophy, but milder and not a genetic lethal. Compare: Duchenne dystrophy. Synonym: Becker type tardive muscular dystrophy. (05 Mar 2000) |
| Becker's muscular dystrophy | An X-linked inherited disorder characterised by slowly progressive muscle weakness of the legs and pelvis. Other symptoms and findings include increased difficulty walking, intellectual retardation, fatigue and pseudohypertrophy of the calf muscles. (27 Sep 1997) |
| Becker type muscular dystrophy | A muscular dystrophy that has many of the clinical features of Duchenne muscular dystrophy e.g., symmetrical involvement of first the pelvicrural muscles and then the pectoral girdle and proximal upper extremity muscles; pseudohypertrophy, especially of the calf muscles but with a much later age of onset (35-45 years), and more benign course. X-linked inheritance. (05 Mar 2000) |
| Becker type tardive muscular dystrophy | Muscular dystrophy of late onset, often in the second or third decade, with relatively mild course; X-linked recessive inheritance; perhaps allelic with Duchenne's dystrophy, but milder and not a genetic lethal. Compare: Duchenne dystrophy. Synonym: Becker type tardive muscular dystrophy. (05 Mar 2000) |
| benign pseudohypertrophic muscular dystrophy | <neurology> An X-linked inherited disorder characterised by slowly progressive muscle weakness of the legs and pelvis. Other symptoms and findings include increased difficulty walking, intellectual retardation, fatigue and pseudohypertrophy of the calf muscles. (06 Aug 1998) |
| pelvofemoral muscular dystrophy | One of the less well-defined types of muscular dystrophy, probably heterogenous in nature. Onset usually in childhood or early adulthood and both sexes affected. Characterised by weakness and wasting, usually symmetrical, of the pelvic girdle muscles, the shoulder girdle muscles, or both, but not the facial muscles. Muscle pseudohypertrophy, heart involvement, and mental retardation are absent. Variable inheritance. Synonym: Leyden-Mobius muscular dystrophy, pelvofemoral muscular dystrophy, scapulohumeral muscular dystrophy. (05 Mar 2000) |