| CAV | congenital absence of vagina; congenital adrenal virilism; constant angular velocity; croup-associat... |
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| CC | calcaneal-cuboid; calcium cyclamate; cardiac catheterization; cardiac contusion; cardiac cycle; card... |
| CHA | Canadian Hospital Association; Catholic Health Association; Chinese hamster; chronic hemolytic anemi... |
| CHD | Chediak-Higashi disease; childhood disease; chronic hemodialysis; congenital or congestive heart dis... |
| CAH | 1) Chronic Active Hepatitis 2) Congenital Adrenal Hyperplasia |
| stricture, oesophagus, acute | A narrowing or closure of the normal opening of the swallowing tube leading to the stomach, usually caused by scarring from acid irritation. Acute, complete obstruction of the oesophagus occurs when food (usually meat) is lodged in the oesophageal stricture. Patients experience chest pain, and are unable to swallow saliva. Attempts to relieve the obstruction by inducing vomiting at home are usually unsuccessful. Patients with complete oesophageal obstruction can breathe, and are not at any risk of suffocation. Endoscopy is usually employed to retrieve the meat and relieve the obstruction. (12 Dec 1998) |
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| stricture of the oesophagus, chronic | A narrowing or closure of the normal opening of the swallowing tube leading to the stomach, usually caused by scarring from acid irritation. A common complication of chronic gastroesophageal reflux disease (gerd). Several procedures are available for stretching (dilating) the strictures without having to resort to surgery. One of the procedures involves placing a deflated balloon across the stricture at the time of endoscopy. The balloon is then inflated, thereby opening the narrowingcaused by the stricture. Another method involves inserting tapered dilators of different sizes through the mouth into the oesophagus to dilate the stricture. (12 Dec 1998) |
| suspensory ligament of oesophagus | Longitudinal fibre of the oesophagus that attaches to the posterior aspect of the cricoid cartilage of the larynx. Synonym: tendo cricoesophageus, Gillette's suspensory ligament, suspensory ligament of oesophagus. (05 Mar 2000) |
| impressions of oesophagus | Three narrowings of the oesophagus normally demonstrated radiographically following a barium swallow: the upper or pharyngeal oesophageal constriction, at the beginning of the oesophagus, is caused by the cricopharyngeus muscle, often referred to as the superior oesophageal sphincter; the middle or aortic constriction is a left-sided narrowing due to the oesophagus passing the aortic arch; the inferior or diaphragmatic oesophageal constriction corresponds to the passage of the oesophagus through the oesophageal hiatus of the diaphragm. Synonym: impressions of oesophagus. (05 Mar 2000) |
| oesophagus | A long hollow muscular tube that connects the pharynx to the stomach. (27 Sep 1997) |
| oesophagus: scleroderma | <radiology> Females (80%), 35-55 years of age, decreased LES pressure, decreased peristalsis, smooth muscle atrophy with or without loose fibrosis, dermatomyositis may include involvement of upper 1/3 (striated), dysphagia to solids more than liquids (steakhouse syndrome), wide-open LES or HH, with or without basilar pulmonary fibrosis, other GI sites associated with CREST syndrome (12 Dec 1998) |
| thoracic part of oesophagus | The part of the oesophagus between the superior thoracic aperture and the diaphragm. Synonym: pars thoracica oesophagi. (05 Mar 2000) |
| feline oesophagus | <radiology> Multiple thin transverse folds seen on oesophagram, normal variant, may be secondary to, GE reflux, scleroderma (12 Dec 1998) |
| adrenal hyperplasia, congenital | A group of inherited disorders of adrenal steroidogenesis, the physical expression of which varies with the sex of the patient, the severity of the congenital enzyme defect, and the age at which the defect makes its presence felt. The most common form, the simple virilizing form, is due to a 21-hydroxylase deficiency. There is also a salt-losing form (a more complete 21-hydroxylase deficiency), a hypertensive form (11-hydroxylase deficiency), a 17-hydroxylase deficiency form, a desmolase deficiency form, and a 3-beta-hydroxysteroid deficiency form. (12 Dec 1998) |
| anaemia, dyserythropoietic, congenital | A familial disorder characterised by anaemia with multinuclear erythroblasts, karyorrhexis, asynchrony of nuclear and cytoplasmic maturation, and various nuclear abnormalities of bone marrow erythrocyte precursors. Type II is the most common of the 3 types of congenital dyserythropoietic anaemia; it is often referred to as hempas, based on the hereditary erythroblast multinuclearity with positive acidified serum test. (12 Dec 1998) |
| anaemia, haemolytic, congenital | Haemolytic anaemia due to various intrinsic defects of the erythrocyte. (12 Dec 1998) |
| anaemia, haemolytic, congenital nonspherocytic | Any one of a group of congenital haemolytic anaemias in which there is no abnormal haemoglobin or spherocytosis and in which there is a defect of glycolysis in the erythrocyte. In some cases, pyruvate kinase deficiency has been demonstrated; in other cases, glucose-6-phosphate dehydrogenase deficiency has been demonstrated. (12 Dec 1998) |
| bovine congenital ataxia | An autosomal recessive ataxia seen in several European breeds of cattle. (05 Mar 2000) |
| bullous congenital ichthyosiform erythroderma | Diffusely red, eroded skin at birth, with subsequent scaling, tending to improve in later life, characterised by generalised epidermolytic hyperkeratosis and autosomal dominant inheritance. See: epidermolytic hyperkeratosis. Synonym: generalised epidermolytic hyperkeratosis, ichthyismus hystrix, ichthyosis hystrix. (05 Mar 2000) |
| pain insensitivity, congenital | Absence of sensibility to pain or inability to feel pain. The condition is present at birth. (12 Dec 1998) |