| HLD | hepatolenticular degeneration; herniated lumbar disk; Hippel-Lindau disease; hypersensitivity lung d... |
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| INCD | infantile nuclear cerebral degeneration |
| JMD | juvenile macular degeneration |
| MDT | mast [cell] degeneration test; mean dissolution time; median detection threshold; multidisciplinary ... |
| NFD | neurofibrillary degeneration |
| Kuhnt-Junius degeneration | An obsolete eponym for disciform degeneration. Synonym: Kuhnt-Junius disease. (05 Mar 2000) |
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| 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) |
| acute primary haemorrhagic meningoencephalitis | A disease characterised by acute onset of fever, followed by convulsions, delirium, and coma, and associated with perivascular demyelination and haemorrhagic foci in the central nervous system. Synonym: acute primary haemorrhagic meningoencephalitis, Strumpell's disease. (05 Mar 2000) |
| acyclic monoterpene primary alcohol - NADP oxidoreductase | <enzyme> From catmint nepeta racemosa; involved in the biosynthesis of iridoid monoterpenes; oxidises geraniol, nerol, and their 10-hydroxy derivatives in the presence of nadp(+). Registry number: EC 1.1.1.- Synonym: monoterpene primary alcohol - nadp oxidoreductase, ampano (26 Jun 1999) |
| anterior primary division | <anatomy, nerve> The larger, anterolaterally-directed major terminal branch (with the dorsal primary ramus) of all 31 pairs of mixed spinal nerves, formed at the intervertebral foramen. Most ventral primary rami, especially those involved in the innervation of the limbs, participate in the formation of the major nerve plexuses (cervical, brachial, and lumbosacral) and lose their identities. Most in the thoracic region, however, remain separate from adjacent rami to become the intercostal and subcostal nerves. Ventral primary rami provide innervation to the anterolateral body wall and trunk. Nomina Anatomica lists ventral primary rami as "rami ventrales" for each group of spinal nerves: 1) cervical (nervorum cervicalium ), 2) thoracic (nervorum thoracicorum ), 3) lumbar (nervorum lumbalium ), 4) sacral (nervorum sacralium )m, and 5) coccygeal (nervi coccygei ). Synonym: ramus ventralis nervi spinalis, anterior primary division. (05 Mar 2000) |
| aphasia, primary progressive | A type of aphasia appearing gradually and gradually worsening without any major change in other cognitive functions. It is regarded by some authors as a syndrome which may be due to various degenerative diseases of the cerebral cortex (notably alzheimer disease, owing to its frequency), while others see in it an autonomous disease related to a neuropathological process that is distinct from the main degenerative dementias. The principal clinical peculiarity of primary progressive aphasia is that it spares the patient's autonomy for a long time, but ultimately turns into global dementia. (12 Dec 1998) |
| ventral primary rami of cervical spinal nerves | See: ventral primary ramus of spinal nerve. Synonym: rami ventrales nervorum cervicalium. (05 Mar 2000) |
| ventral primary rami of lumbar spinal nerves | See: ventral primary ramus of spinal nerve. Synonym: rami ventrales nervorum lumbalium. (05 Mar 2000) |
| ventral primary rami of sacral spinal nerves | See: ventral primary ramus of spinal nerve. Synonym: rami ventrales nervorum sacralium. (05 Mar 2000) |
| ventral primary ramus of spinal nerve | <anatomy, nerve> The larger, anterolaterally-directed major terminal branch (with the dorsal primary ramus) of all 31 pairs of mixed spinal nerves, formed at the intervertebral foramen. Most ventral primary rami, especially those involved in the innervation of the limbs, participate in the formation of the major nerve plexuses (cervical, brachial, and lumbosacral) and lose their identities. Most in the thoracic region, however, remain separate from adjacent rami to become the intercostal and subcostal nerves. Ventral primary rami provide innervation to the anterolateral body wall and trunk. Nomina Anatomica lists ventral primary rami as "rami ventrales" for each group of spinal nerves: 1) cervical (nervorum cervicalium ), 2) thoracic (nervorum thoracicorum ), 3) lumbar (nervorum lumbalium ), 4) sacral (nervorum sacralium )m, and 5) coccygeal (nervi coccygei ). Synonym: ramus ventralis nervi spinalis, anterior primary division. (05 Mar 2000) |
| Ghon's primary lesion | Calcification seen in pulmonary parenchyma (usually mid-lung area) and hilar nodes resulting from earlier, usually childhood, infection with tuberculosis. Synonym: Ghon's complex, Ghon's focus, Ghon's primary lesion. (05 Mar 2000) |
| persistent anterior hyperplastic primary vitreous | A unilateral congenital abnormality occurring in full-term infants; characterised by a retrolental fibrovascular membrane formed by persistent primary vitreous with remnants of the hyaloid artery and tunica vasculosa lentis; associated with leukokoria, microphthalmos, shallow anterior chamber, and elongated ciliary processes. (05 Mar 2000) |