| ACHOO | autosomal dominant compelling helio-ophthalmic outburst [syndrome] |
|---|---|
| AD | accident dispensary; acetate dialysis; active disease; acute dermatomyositis; addict, addiction; ade... |
| ADPKD | autosomal dominant polycystic kidney disease |
| ADVIRC | autosomal dominant vitreo-retinochoroidopathy |
| TDFA | testis-determining factor, autosomal |
| sphincter of hepatic flexure of colon | Physiological sphincter at the level of the right colic flexure. (05 Mar 2000) |
|---|---|
| nervous colon syndrome | <syndrome> A common gastrointestinal disorder characterised by abdominal pain, bloating, mucous in stools, and irregular bowel habits with alternating diarrhoea and constipation, symptoms that tend to be chronic and wax and wane over the years. Although nervous colon syndrome can cause chronic recurrent discomfort, it appears to be an abnormal condition of gut contractions (motility) and does not lead to any serious organ problems. Diagnosis usually involves excluding other illnesses. Treatment is directed toward relief of symptoms and includes high fibre diet, exercise, relaxation techniques, avoidance of caffeine, milk products and sweeteners, and medications. Alternative names include irritable bowel syndrome, spastic colitis, and mucus colitis. (12 Dec 1998) |
| syndrome, nervous colon | See Syndrome, irritable bowel. (12 Dec 1998) |
| descending colon | The fourth portion of the large intestine (colon) that communicates with the transverse colon in the left-upper quadrant of the abdomen and the rectum below. (27 Sep 1997) |
| diverticula of colon | Diverticula, which are herniations of mucosa and submucosa through or between fibres of the major muscle layer (muscularis propria) of the colon. Usually multiple, it occurs in 50% of western populations above the age of 70, but is much less common in other populations. Can cause bleeding and episodes of severe inflammation. Synonym: colonic diverticula. (05 Mar 2000) |
| diverticular disease of colon | <radiology> Overactivity of smooth muscle causing herniation of mucosa and submucosa through the muscle layers, incidence: 5-10% in 5th decade; 50% past 7th decade; M:F = 1:1, aetiology: decreased faecal bulk; diet high in refined fibre and low in roughage, location: sigmoid (80%): narrowest colonic segment with highest pressure, entire colon (17%), caecum/ascending colon (4-12%) see also: prediverticular disease of colon, colonic diverticulosis, colonic diverticulitis, colonic diverticular hemmorrhage (12 Dec 1998) |
| iliac colon | That portion of the descending colon which occupies the left iliac fossa, between the crest of the left ilium and the pelvic brim. Irritable colon, tendency to colonic hyperperistalsis, sometimes with colicky pains and diarrhoea. Lead-pipe colon, the scarred rigid colon of advanced ulcerative colitis. Mucosa of colon, the lining coat of the colon. Synonym: tunica mucosa coli. (05 Mar 2000) |
| irritable colon | A functional bowel disorder characterised by recurrent crampy abdominal pain and diarrhoea. Invasive gastrointestinal diagnostics are often unrevealing. (27 Sep 1997) |
| transverse colon | <anatomy> The third division of the colon (large intestine). It communicates with the ascending colon in the upper right-hand quadrant of the abdomen and the descending colon in the upper left-hand quadrant. (19 Jan 1998) |
| benign familial chorea | A rare, nonprogressive movement disorder characterised by chorea and athetosis appearing in early childhood, most commonly manifested as gait ataxia and upper limb coordination. Intellect is unaffected. Probably autosomal-dominance inheritance with incomplete penetrance. (05 Mar 2000) |
| benign familial chronic pemphigus | Recurrent eruption of vesicles and bullae that become scaling and crusted lesions with vesicular borders, predominantly of the neck, groin, and axillary regions; autosomal dominant inheritance, presenting in late adolescence or early adult life. Synonym: Hailey-Hailey disease. (05 Mar 2000) |
| benign familial icterus | Mild jaundice due to increased amounts of unconjugated bilirubin in the plasma without evidence of liver damage, biliary obstruction, or haemolysis; thought to be due to an inborn error of metabolism in which the excretion of bilirubin by the liver is defective, ascribed to decreased conjugation of bilirubin as a glucuronide or impaired uptake of hepatic bilirubin. Synonym: benign familial icterus, constitutional hepatic dysfunction, Gilbert's disease, Gilbert's syndrome, Hebra's disease. (05 Mar 2000) |
| cancer, breast, familial | A number of factors have been identified that increase the risk of breast cancer. One of the strongest of these risk factors is the history of breast cancer in a relative. About 15-20% of women with breast cancer have such a family history of the disease, clearly reflecting the participation of inherited (genetic) components in the development of some breast cancers. Dominant breast cancer suceptibility genes, including BRCA1 and BRCA2, appear responsible for about 5% of all breast cancer. (12 Dec 1998) |
| paralysis, familial periodic | An autosomal dominant trait marked by recurring attacks of rapidly progressive flaccid paralysis. There are three types: I, associated with a fall in serum potassium levels (hypokalaemic periodic paralysis); II, associated with a rise therein (hyperkalaemic periodic paralysis, called also adynamia episodica hereditaria); and III, with normal levels (normokalaemic periodic paralysis). (12 Dec 1998) |
| pemphigus, benign familial | Rare hereditary disease characterised by recurrent eruptions of vesicles and bullae mainly on the neck, axillae, and groin. It exhibits autosomal dominant inheritance and is unrelated to pemphigus vulgaris though it closely resembles that disease. (12 Dec 1998) |