| AIDP | acute idiopathic demyelinating polyneuropathy |
|---|---|
| CIPN | chronic inflammatory polyneuropathy |
| CPN | central parenteral nutrition; chronic polyneuropathy; chronic pyelonephritis |
| CR-DIP | chronic relapsing demyelinating inflammatory polyneuropathy |
| DPN | dermatosis papulosa nigra; diabetic polyneuropathy; diphosphopyridine nucleotide; disabling panscler... |
| hypertrophic interstitial neuropathy | Sensorimotor neuropathy characterised pathologically by collections of Schwann cell processes arranged concentrically around one or more nerve fibres. No genetic factors are known in its aetiology.For hereditary types, see hereditary hypertrophic neuropathy. (05 Mar 2000) |
|---|---|
| hypertrophic osteoarthropathy | <radiology> Pulmonary, malignancy (bronchogenic carcinoma, lymphoma, metastasis), abscess, COPD / bronchiectasis, pleural, pleural fibroma (highest incidence of HOA, tho' rare itself), mesothelioma, cardiac, cyanotic congenital heart disease, GI, inflammatory disease (Crohn, UC), malabsorption (dysentery, lue, cirrhosis), ** causes symmetrical periosteal reaction (12 Dec 1998) |
| hypertrophic pyloric stenosis | <radiology> Not seen until 3 weeks, projectile vomiting, palpable olive in RUQ/epigastrium (12 Dec 1998) |
| hypertrophic rhinitis | Chronic rhinitis with permanent thickening of the mucous membrane. (05 Mar 2000) |
| hypertrophic rosacea | A manifestation of severe acne rosacea resulting in significant enlargement of the nose and occurring primarily in men. It is caused by hypertrophy of the sebaceous glands and surrounding connective tissue. The nose is reddened and marked with numerous telangiectasias. (12 Dec 1998) |
| hypertrophic scar | An elevated scar resembling a keloid but which does not spread into surrounding tissues, is rarely painful, and regresses spontaneously; collagen bundles run parallel to the skin surface. (05 Mar 2000) |
| idiopathic hypertrophic subaortic stenosis | <cardiology> A congenital heart disease that results in abnormal thickening of the ventricular septum and left ventricular wall. Enlargement of the ventricular septum can result in ventricular outflow obstruction (subaortic stenosis) and eventual cardiomyopathy. (27 Sep 1997) |
| osteoarthropathy, primary hypertrophic | A conditioned chiefly characterised by thickening of the skin of the head and distal extremities, deep folds and furrows of the skin of the forehead, cheeks, and scalp, seborrhoea, hyperhidrosis, periostosis of the long bones, digital clubbing, and spadelike enlargement of the hands and feet. It is more prevalent in the male, and is usually first evident during adolescence. It is believed to be inherited as an autosomal dominant trait. (12 Dec 1998) |
| osteoarthropathy, secondary hypertrophic | Symmetrical osteitis of the four limbs, chiefly localised to the phalanges and the terminal epiphyses of the long bones of the forearm and leg, sometimes extending to the proximal ends of the limbs and the flat bones, and accompanied by dorsal kyphosis and joint involvement. It is often secondary to chronic conditions of the lungs and heart. (12 Dec 1998) |
| familial hypertrophic cardiomyopathy | Familial occurrence of hypertrophic cardiomyopathy exhibiting an autosomal dominant pattern of inheritance. Familial cardiomyopathy of various kinds occurs with autosomal dominant inheritance. There is also an asymmetrical form affecting the ventricles and the interventricular septum. (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) |
| bovine progressive degenerative myeloencephalopathy | A familiar myeloencephalopathy of brown Swiss cattle characterised by bilateral hindleg weakness and ataxia and deficient proprioceptive reflexes. (05 Mar 2000) |
| rapidly progressive glomerulonephritis | <nephrology> A relatively uncommon (affecting 1 out of 10,000 people) form of acute glomerulonephritis that results in damage within the glomerulus of the kidney. There is rapid loss of kidney function with the formation of crescents on microscopic analysis (kidney biopsy). This disorder may result in acute glomerulonephritis or nephrotic syndrome, but ultimately results in renal failure and end-stage renal disease. Symptoms include smoky coloured urine (pyuria), decreased urine output, swelling and hypertension. Any conditions which can cause a vasculitis increase the risk of this disorder. Some examples include lupus, Goodpasture's syndrome, Henoch-Schonlein purpura, IgA nephropathy, membranoproliferative glomerulonephritis, anti-glomerular basement membrane antibody disease, history for malignant tumours and exposure to hydrocarbon solvents. (27 Sep 1997) |
| chronic progressive chorea | A progressive disorder usually beginning in young to middle age, consisting of a triad of choreoathetosis, dementia, and autosomal dominant inheritance with complete penetrance. Bilateral marked wasting of the putamen and the head of the caudate nucleus is characteristic. Synonym: chronic progressive chorea, degenerative chorea, hereditary chorea, Huntington's disease. (05 Mar 2000) |
| chronic progressive external ophthalmoplegia | A specific type of slowly worsening weakness of the ocular muscles, usually associated with a pigmentary retinopathy. See: Kearns-Sayre syndrome, oculopharyngeal dystrophy. Synonym: ocular myopathy. (05 Mar 2000) |