| PFKL | phosphofructokinase, liver type; 6-phosphofructo-2-kinase, liver type |
|---|---|
| PFKP | phosphofructokinase, platelet type; 6-phosphofructo-2-kinase, platelet type |
| MAT | Multifocal Atrial Tachycardia |
| PVC | Premature Ventricular Contraction(s) = VEB ? Ix of Tx ... |
| CRMO | chronic recurrent multifocal osteomyelitis |
| subacute spongiform encephalopathy | A form of spongiform encephalopathy that is associated with a "slow virus", which to date has not been adequately described, is transmissible, and has a rapidly progressive, fatal course; e.g., Creutzfeldt-Jakob disease, kuru, Gerstmann-Straussler syndrome, scrapie. (05 Mar 2000) |
|---|---|
| subcortical arteriosclerotic encephalopathy | One of the causes of multiinfarct dementia, in which there are many infarcts and lacunes in the white matter, with relative sparing of the cortex and basal ganglia. Synonym: Binswanger's encephalopathy, encephalitis subcorticalis chronica, subcortical arteriosclerotic encephalopathy. (05 Mar 2000) |
| demyelinating encephalopathy | Extensive idiopathic loss of myelin sheaths in the brain, as occurs in leukodystrophy. (05 Mar 2000) |
| dialysis encephalopathy syndrome | <syndrome> A progressive (often fatal) diffuse encephalopathy which occurs in a few patients who undergo chronic haemodialysis, dementia is a key feature (27 Sep 1997) |
| thyrotoxic encephalopathy | A metabolic encephalopathy arising in severe cases of thyrotoxicosis. (05 Mar 2000) |
| encephalopathy | <neurology, pathology> Any degenerative disease of the brain. Origin: Gr. Pathos = disease (18 Nov 1997) |
| encephalopathy, bovine spongiform | Scrapie-like neurological disorder of cattle. The infection appears to be caused by the consumption of scrapie-infected ruminant-derived protein (prions). (12 Dec 1998) |
| transmissible mink encephalopathy | <virology> Unconventional type of slow virus infection, similar to kuru, scrapie and Creutzfeldt Jakob disease. See: prion. Origin: Gr. Pathos = disease (18 Nov 1997) |
| traumatic encephalopathy | An encephalopathy resulting from structural brain injury. (05 Mar 2000) |
| traumatic progressive encephalopathy | A chronic progressive brain damage resulting from multiple brain injuries, e.g., dementia pugilistica. (05 Mar 2000) |
| lead encephalopathy | A metabolic encephalopathy, caused by the ingestion of lead compounds and seen particularly in early childhood; it is characterised pathologically by extensive cerebral oedema, status spongiosus, neurocytolysis, and some reactive inflammation; clinical manifestations include convulsions, delirium, and hallucinations. See: lead poisoning. Synonym: lead encephalitis, saturnine encephalopathy. (05 Mar 2000) |
| acrocephalosyndactyly type 1 | <paediatrics> An inherited disease (autosomal dominant) or a spontaneously occurring disease characterised by a peaked head and unusual facial appearance, due to the premature closure of the cranial sutures. A skull X-ray can confirm the diagnosis and treatment is surgical. Inheritance: autosomal dominant. (27 Sep 1997) |
| Alzheimer type I astrocyte | Enlarged frequently multinucleated astrocytes, seen in progressive multifocal leukoencephalopathy. (05 Mar 2000) |
| Alzheimer type II astrocyte | Enlarged astrocytes with vesicular nuclei and one or more small basophilic nucleoli, seen in hepatocerebral disease and Wilson's disease. (05 Mar 2000) |
| American Type Culture Collection | <cell culture> A key resource for cultured cells, located in Rockville, USA. (12 Dec 1998) |