| EA | 1) Esophageal Atresia Types 1. Esophageal Atresia with Dis... |
|---|---|
| BA | Bachelor of Arts; backache; bacterial agglutination; basilar artery; basion; benzyladenine; best amp... |
| EHBA | extrahepatic biliary atresia |
| VATER Associations | Vertebral defects Anal atresia Tracheo-Esophageal fistula ... |
| VACTERL | vertebral abnormalities, anal atresia, cardiac abnormalities, tracheoesophageal fistula and/or esoph... |
| BA | Biliary atresia |
|---|---|
| EHBA | Extra Hepatic Biliary Atresia |
| EA | Esophageal atresia |
| OA | Oesophageal atresia |
| PA | Pulmonary atresia |
| 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) |
|---|
| 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) |
| 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) |
| oesophageal atresia | A congenital anomaly where the upper oesophagus ends (atresia) and does not connect with the stomach and the lower oesophagus connects to the trachea (tracheoesophageal fistula). A common complication seen shortly after birth is an aspiration pneumonia. Infants will demonstrate excessive salivation, gagging and coughing with feeding, poor feeding and a bluish discolouration to the skin (cyanosis). Treatment involves the surgical repair of the oesophagus before the child can take anything by mouth. (27 Sep 1997) |
| tricuspid atresia | Absence of the orifice between the right atrium and ventricle, with the presence of an atrial defect through which all the systemic venous return reaches the left heart. As a result, there is left ventricular hypertrophy (hypertrophy, left ventricular) because the right ventricle is absent or not functional. (12 Dec 1998) |
| follicular atresia | <physiology> The degeneration and resorption of an ovarian follicle before it reaches maturity and ruptures. (12 Dec 1998) |
| laryngeal atresia | Congenital failure of the laryngeal opening to develop, resulting in partial or total obstruction at or just above or below the glottis. (05 Mar 2000) |
Synonyms :
| biliary atresia |
obliteration or hypoplasia of one or more components of the bile ducts due to arrested fetal development, resulting in persistent jaundice and liver damage ranging from biliary stasis to biliary cirrhosis, with splenomegaly as portal hypertension progresses.
Ãâó: www.mercksource.com/pp/us/cns/cns_hl_dorlands.jspz...
|
|---|---|
| biliary atresia |
a birth defect in which the bile ducts are not completely developed; often a liver transplant is necessary
Ãâó: www.american-depot.com/services/resources_gl_b.asp
|
| biliary atresia |
condition present from birth in which the bile ducts inside or outside the liver do not have normal openings. Bile becomes trapped in the liver, causing jaundice and cirrhosis. Without surgery, the condition may cause death.
Ãâó: ymghealthinfo.org/content.asp
|
| biliary atresia |
bile ducts do not have normal openings, preventing bile from leaving the liver. This causes jaundice (yellowing of skin or eyes) and liver damage known as cirrhosis. Biliary atresia is a birth defect.
Ãâó: www.uchicagokidshospital.org/online-library/conten...
|
| biliary atresia |
Congenital condition in which bile from the liver cannot reach the intestine because the bile ducts have developed poorly or not at all
Ãâó: www.tigerfund.org/glossary.htm
|
Á¦Ç°¸í |
ÆÇ¸Å»ç |
º¸ÇèÄÚµå | ¼ººÐ/ÇÔ·® | ±¸ºÐ/º¸Çè±Þ¿© |
|---|
Á¦Ç°¸í |
ÆÇ¸Å»ç |
º¸ÇèÄÚµå | ¼ººÐ/ÇÔ·® | ±¸ºÐ/º¸Çè±Þ¿© |
|---|