| 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 |
| primary progressive cerebellar degeneration | A familial ataxic condition related to cerebellar degeneration. (05 Mar 2000) |
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| Salzmann's nodular corneal degeneration | Large and prominent nodules of a solid, opaque material that stands out from the surface of the cornea; occurs occasionally in persons previously affected by phlyctenular keratitis. (05 Mar 2000) |
| hepatolenticular degeneration | <gastroenterology, neurology> An inherited 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) |
| xerotic degeneration | Scarring of the conjunctiva associated with keratinised epithelium. (05 Mar 2000) |
| pseudotubular degeneration | A form of degeneration observed in adrenal glands, especially those of patients with febrile infectious disease; the shrunken, lipid-depleted cells of the zona fasciculata (and sometimes the zona glomerulosa) are arranged in a circular pattern about spaces that may be empty or partly filled with fibrin, necrotic cells, or amorphous material. (05 Mar 2000) |
| secondary degeneration | <medicine> A form of degeneration occurring in nerve fibres as a result of their division; so called from Dr. Waller, who published an account of it in 1850. Source: Websters Dictionary (01 Mar 1998) |
| senile degeneration | The process of involution occurring in old age. (05 Mar 2000) |
| hyaline degeneration | A group of several degenerative processes that affect various cells and tissues, resulting in the formation of rounded masses ("droplets") or relatively broad bands of substances that are homogeneous, translucent, refractile, and moderately to deeply acidophilic; may occur in the collagen of old fibrous tissue, smooth muscle of arterioles or the uterus, and as droplets in parenchymal cells. (05 Mar 2000) |
| hyaline degeneration of the elastic tissue of the arterial wall | Seen during involution of the uterus. (05 Mar 2000) |
| hyaloideoretinal degeneration | Progressive liquefaction and destruction of the vitreous humor with grayish-white preretinal membranes, myopia, cataract, retinal detachment, and hyper-and hypopigmentation; autosomal dominant inheritance. Synonym: Wagner's disease, Wagner's syndrome. (05 Mar 2000) |
| hydropic degeneration | Swelling of cells due to injury to the membranes affecting ionic transfer; causes an accumulation of intracellular water. Synonym: albuminous swelling, granular degeneration, hydropic degeneration, parenchymatous degeneration. (05 Mar 2000) |
| Sorsby's macular degeneration | Macular degeneration that occurs during the fifth decade of life, with sudden development of a central scotoma in one eye followed rapidly by a similar lesion in the opposite eye; autosomal dominant inheritance. Synonym: Sorsby's macular degeneration. (05 Mar 2000) |
| spinocerebellar degeneration | An autosomal recessive inherited disorder that leads to the progressive dysfunction of the cerebellum, spinal cord and peripheral nerves. Symptoms usually begin in childhood before puberty and consist of an unsteady gait (ataxia), slurred speech (dysarthria) and jerky eye movements (nystagmus). Other findings include kyphoscoliosis, hammer toe, heart disease and high arches. Congestive heart failure is a common complication. There is no known treatment and prognosis is poor. Inheritance: autosomal recessive. (27 Sep 1997) |
| spongy degeneration | <radiology> (Canavan disease) dysmyelinating disease, autosomal recessive, onset at 2 - 9 months, megalencephaly, (Alexander disease only other degenerative neurological disease in infants with big head!), blindness with or without deafness, hypotonia may lead to spasticity, Diagnosis: brain biopsy, centrum semiovale most severely affected (12 Dec 1998) |
| spongy degeneration of infancy | Autosomal recessive degenerative disease of infancy; mostly in Jewish infants; onset typically within first 3-4 months of birth, consisting of blindness, psychomotor regression, enlarged head, optic atrophy, hypotonia, spasticity, increased N-acetylaspartic acid urinary excretion. MRI shows enlarged brain, decreased attenuation of cerebral and cerebellar white matter, and normal ventricles. Pathologically, there is increased brain volume and weight, and spongy degeneration in the subcortical white matter. See: leukodystrophy. Synonym: Canavan's sclerosis, Canavan-van Bogaert-Bertrand disease, spongy degeneration of infancy. (05 Mar 2000) |