| RED | radiation experience data; rapid erythrocyte degeneration |
|---|---|
| SACD | subacute combined degeneration |
| SDC | serum digoxin concentration; Smith delay compensator; sodium deoxycholate; subacute combined degener... |
| SDSEM | spinocerebellar degeneration-slow eye movements [syndrome] |
| SMD | senile macular degeneration; spondylometaphyseal dysplasia; submanubrial dullness |
| Kuhnt-Junius degeneration | An obsolete eponym for disciform degeneration. Synonym: Kuhnt-Junius disease. (05 Mar 2000) |
|---|---|
| fibrinous degeneration | A process resulting in poorly defined, deeply acidophilic, homogeneous refractile deposits with some staining reactions that resemble fibrin, occurring in connective tissue, blood vessel walls, and other sites. (05 Mar 2000) |
| fibrous degeneration | Not a degeneration per se, but rather a reparative process; cells and foci of tissue previously affected with degenerative processes, and necrosis, are replaced by cellular fibrous tissue. (05 Mar 2000) |
| lenticular progressive degeneration | <gastroenterology, neurology> An inherited (autosomal recessive) disorder where there is excessive quantities of copper in the tissues, particularly the liver and central nervous system. Wilson's disease causes the body to absorb and retain copper. The copper deposits in the liver, brain, kidneys and eyes. Complications include dementia and liver failure. Symptoms include jaundice, vomiting, tremors, weakness and slow stiff movements. Blood tests show serum ceruloplasmin is low. Medications are given to remove the excess copper from the body. Even with life-long treatment, disabling (and life-threatening) side effects are common. Inheritance: autosomal recessive. (27 Sep 1997) |
| liquefaction degeneration | Necrosis with softening, as in ischemic brain tissue, dissolution of the basal epidermal layer by necrosis of scattered cells with oedema, observed in lichen planus, lupus erythematosus, and other dermatologic conditions. (05 Mar 2000) |