| FIMG | familial infantile myasthenia gravis |
|---|---|
| IA | ibotenic acid; immune adherence; immunoadsorbent; immunobiologic activity; impedance angle; indolami... |
| IAFI | infantile amaurotic familial idiocy |
| IBSN | infantile bilateral striated necrosis |
| ICP | incubation period; indwelling catheter program; infantile cerebral palsy; infection-control practiti... |
| progressive cataract | A cataract in which the opacification process progresses to involve the entire lens. (05 Mar 2000) |
|---|---|
| progressive cerebellar tremor | <syndrome> An intention tremor beginning in one extremity, gradually increasing in intensity, and subsequently involving other parts of the body. Synonym: progressive cerebellar tremor. Facial paralysis, otalgia, and herpes zoster resulting from viral infection of the seventh cranial nerve and geniculate ganglion, a form of juvenile paralysis agitans associated with primary atrophy of the pallidal system. Synonym: paleostriatal syndrome, pallidal syndrome. Synonym: Ramsay Hunt's syndrome. (05 Mar 2000) |
| progressive cerebral poliodystrophy | Familial progressive spastic paresis of extremities with progressive mental deterioration, with development of seizures, blindness and deafness, beginning during the first year of life, and with destruction and disorganization of nerve cells of the cerebral cortex. Synonym: Alpers disease, Christensen-Krabbe disease, progressive cerebral poliodystrophy. (05 Mar 2000) |
| progressive cleavage | In fungi, a type of sporulation in which cleavage planes in the cytoplasm first produce protospores and then sporangiospores in a sporangium. (05 Mar 2000) |
| progressive emphysematous necrosis | <microbiology> A severe form of gangrene (tissue necrosis) caused by Clostridium infection. Also referred to as necrotising subcutaneous infection. Results in death of the subcutaneous tissues and muscle layers. See: necrotising fascitis. (27 Sep 1997) |
| progressive familial scleroderma | A syndrome characterised by calcinosis cutis, Raynaud's phenomenon, sclerodactyly, and telangiectasia; usually due to scleroderma; autosomal dominant form of progressive systemic sclerosis. (05 Mar 2000) |
| progressive hypertrophic polyneuropathy | A familial type of demyelinating sensorimotor polyneuropathy that begins in early childhood and is slowly progressive; clinically characterised by foot pain and paresthesias, followed by symmetrical weakness and wasting of the distal limbs; one of the causes of stork legs; patients are wheelchair bound at an early age; peripheral nerves are palpably enlarged and non-tender; pathologically, onion bulb formation is seen in the nerves: whorls of overlapping, intertwined Schwann cell processes that encircle bare axons; usually autosomal recessive inheritance. Synonym: Dejerine's disease, progressive hypertrophic polyneuropathy. (05 Mar 2000) |
| progressive lipodystrophy | A condition characterised by a complete loss of the subcutaneous fat of the upper part of the torso, the arms, neck, and face, sometimes with an increase of fat in the tissues about and below the pelvis. Synonym: Barraquer's disease, lipodystrophia progessiva superior, partial lipoatrophy, Simons' disease. (05 Mar 2000) |
| progressive massive fibrosis | <radiology> Progressive massive fibrosis, silicosis (properly conglomerate nodules, not progressive massive fibrosis), coal worker's pneumoconiosis, density (conglomerate mass) in upper lobe, retracts toward hilum, leaves emphysematous change (bullae) at lung periphery (12 Dec 1998) |
| progressive multifocal leukoencephalopathy | <radiology> Demyelinating disease due to papovavirus, seen in immunosuppressed hosts: lymphoma, leukaemia, AIDS, TB, sarcoidosis, organ transplant, most prominent in pareito-occipital white matter, NO contrast enhancement (12 Dec 1998) |
| progressive muscle relaxation | A cognitive-behavioural strategy in which muscles are alternately tensed and then relaxed in a systematic fashion. (16 Dec 1997) |
| progressive patient care | Organization of medical and nursing care according to the degree of illness and care requirements in the hospital. The elements are intensive care, intermediate care, self-care, long-term care, and organised home care. (12 Dec 1998) |
| progressive pigmentary dermatosis | Chronic purpura, especially of the legs in men, spreading to form brownish patches; associated microscopically with perivascular lymphatic infiltration, diapedesis, and haemosiderosis. Synonym: Schamberg's dermatitis. (05 Mar 2000) |
| progressive pneumonia | A chronic progressive, viral disease of sheep and goats manifested as maedi or visna in different parts of the world. See: maedi, visna. (05 Mar 2000) |
| progressive pneumonia virus | A retrovirus (subfamily Lentivirinae) that is the cause of maedi; it is very similar to the visna virus Synonym: medi virus, progressive pneumonia virus. (05 Mar 2000) |