| COFS | cerebro-oculo-facial-skeletal [syndrome] |
|---|---|
| FFDD | focal facial dermal dysplasia |
| FH | facial hemihyperplasia; familial hypercholesterolemia; family history; fasting hyperbilirubinemia; f... |
| GP | gangliocytic paraganglioma; gastroplasty; general paralysis, general paresis; general practice, gene... |
| GPI | general paralysis of the insane; glucose phosphate isomerase; glycoprotein I; glycosylphosphatidylin... |
| diaphyseal dysplasia, progressive | Progressive thickening of diaphyseal cortex of long bones. (12 Dec 1998) |
|---|---|
| infantile progressive spinal muscular atrophy | Transmitted as autosomal recessive on chromosome 5q. Progressive dysfunction of the anterior horn cells in the spinal cord and brainstem cranial nerves with profound weakness and bulbar dysfunction occurring in the first two years of life. Three groups, based on age of clinical onset, are recognised. Synonym: familial spinal muscular atrophy, Hoffmann's muscular atrophy, infantile muscular atrophy, infantile progressive spinal muscular atrophy, progressive infantile spinal muscular atrophy, Werdnig-Hoffmann disease, Werdnig-Hoffmann muscular atrophy. (05 Mar 2000) |
| ophthalmoplegia, chronic progressive external | One of the mitochondrial encephalomyopathies characterised by slowly progressive paralysis of the extraocular muscles. Muscle biopsies disclose the characteristic ragged red fibres and large numbers of mitochondria with deleted DNA. (12 Dec 1998) |
| ovine progressive pneumonia | A chronic, progressive, contagious interstitial pneumonitis of sheep in Europe and the U.S. Caused by a "slow virus" (family Lentiviridae); it is now believed that maedi and visna are two histopathological and clinical manifestations of the same viral infection. Synonym: ovine progressive pneumonia. Origin: Icelandic, dyspnea (05 Mar 2000) |
| traumatic progressive encephalopathy | A chronic progressive brain damage resulting from multiple brain injuries, e.g., dementia pugilistica. (05 Mar 2000) |
| essential progressive atrophy of iris | Progressive atrophy of the iris without inflammatory signs, characterised by patchy loss of all layers of the iris with hole formation, migration of the pupil, degeneration of the corneal endothelium, peripheral anterior synechiae, and secondary glaucoma; usually unilateral, predominantly affecting women in their middle years. (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) |
| leukoencephalopathy, progressive multifocal | Rare demyelinating disease of the central nervous system which develops in immunocompromised patients secondary to lymphoproliferative disease, immunosuppressive therapy, autoimmune disorders, or aids. It is caused by the jc virus, a polyomavirus. (12 Dec 1998) |
| acute ascending paralysis | A paralysis of rapid course beginning in the legs and involving progressively the trunk, arms, and neck, ending sometimes in death in from one to three weeks. Synonym: ascending paralysis. (05 Mar 2000) |
| acute atrophic paralysis | Inflammation of the anterior cornua of the spinal cord; an acute infectious disease caused by the poliomyelitis virus and marked by fever, pains, and gastroenteric disturbances, followed by a flaccid paralysis of one or more muscular groups, and later by atrophy. Synonym: acute atrophic paralysis, myogenic paralysis. (05 Mar 2000) |
| ascending paralysis | A paralysis of rapid course beginning in the legs and involving progressively the trunk, arms, and neck, ending sometimes in death in from one to three weeks. Synonym: ascending paralysis. (05 Mar 2000) |
| ascending tick paralysis | <neurology> An ascending paralysis caused by the continued presence of Dermacentor and Ixodes ticks attached to the occipital or upper neck region in humans. The treatment consists of tick removal and supportive care. (27 Sep 1997) |
| Brown-Sequard's paralysis | <neurology, syndrome> A type of spinal cord lesion that is characterised by hemiparaplegia and hyperesthesia, but with loss of motor function on the same side as the lesion and hemianaesthesia on the opposite side. (27 Sep 1997) |
| bulbar paralysis | Progressive weakness and atrophy of the muscles of the tongue, lips, palate, pharynx, and larynx, usually occurring in later life; most often caused by motor neuron disease. Synonym: bulbar palsy, bulbar paralysis, Duchenne's disease, Erb disease, glossolabiolaryngeal paralysis, glossolabiopharyngeal paralysis. (05 Mar 2000) |
| vasomotor paralysis | A mild degree of vasoparalysis. Synonym: angioparesis, vasomotor paralysis. Origin: vaso-+ G. Paresis, weakness (05 Mar 2000) |