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| EA | 1) Esophageal Atresia Types 1. Esophageal Atresia with Dis... |
|---|---|
| PILBD | paucity of interlobular bile ducts |
| VATER Associations | Vertebral defects Anal atresia Tracheo-Esophageal fistula ... |
| VACTERL | vertebral abnormalities, anal atresia, cardiac abnormalities, tracheoesophageal fistula and/or esoph... |
| BA | Bachelor of Arts; backache; bacterial agglutination; basilar artery; basion; benzyladenine; best amp... |
| BA | Biliary atresia |
|---|---|
| EA | Esophageal atresia |
| EHBA | Extra Hepatic Biliary Atresia |
| OA | Oesophageal atresia |
| PA | Pulmonary atresia |
| aberrant bile ducts | Small duct's occasionally present in the ligaments of the liver or originating from the surface of the liver. (05 Mar 2000) |
|---|---|
| bile ducts, extrahepatic | Passages external to the liver for the conveyance of bile. These include the common bile duct and the common hepatic duct (hepatic duct, common). (12 Dec 1998) |
| bile ducts, intrahepatic | Passages within the liver for the conveyance of bile. Includes right and left hepatic ducts even though these may join outside the liver to form the common hepatic duct. (12 Dec 1998) |
| anal atresia | A congenital obstruction of the anal opening. Occurs in approximately 1 in 5,000 infants. This condition is corrected through surgery. (27 Sep 1997) |
| aortic atresia | Congenital absence of the normal valvular orifice into the aorta. (05 Mar 2000) |
| atresia | <medicine> Absence or closure of a natural passage or channel of the body; imperforation. Origin: NL, fr. Gr. Not perforated. Source: Websters Dictionary (01 Mar 1998) |
| atresia folliculi | A normal process affecting the primordial ovarian follicles in which death of the ovum results in cystic degeneration followed by cicatricial closure. (05 Mar 2000) |
| atresia iridis | Congenital absence of the pupillary opening. Synonym: atretopsia. (05 Mar 2000) |
| biliary atresia | <embryology> A rare condition which is caused by the abnormal development of the bile ducts inside or outside the liver. The obstruction of bile flow from the liver can lead to cirrhosis of the liver if not treated. Symptoms include jaundice in the second to third week of life along with clay-coloured stools. See: newborn jaundice. (27 Sep 1997) |
| bronchial atresia | Severe focal narrowing or obliteration of a segmental or lobar bronchus, usually associated with distal air trapping. (05 Mar 2000) |
| vaginal atresia | Congenital or acquired imperforation or occlusion of the vagina, or adhesion of the walls of the vagina. Synonym: ankylocolpos, colpatresia. (05 Mar 2000) |
| choanal atresia | Congenital bony or membranous occlusion of one or both choanae, due to failure of the embryonic bucconasal membrane to rupture. (12 Dec 1998) |
| pulmonary atresia | Congenital absence of the normal valvular orifice into the pulmonary artery. This condition is characterised by cardiomegaly, reduced pulmonary vascularity, and right ventricular atrophy. (12 Dec 1998) |
| duodenal atresia | <radiology> Double bubble sign, polyhydramnios, associated with, Down syndrome, VATER syndrome NB: annular pancreas also may cause duodenal obstruction, and is associated with VATER syndrome (12 Dec 1998) |
| intestinal atresia | Congenital obliteration of the lumen of the intestine, with the ileum involved in 50% of the cases and the jejunum and duodenum following in frequency. It is the most frequent cause of intestinal obstruction in the newborn infant. Its aetiology may be related to failure of recanalization during early development or to some impairment of blood supply during intrauterine life. (12 Dec 1998) |
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