The CPT code for a single-stage reconstruction of the right external auditory canal due to congenital atresia is typically 69631. This code specifically pertains to procedures involving the reconstruction of the external auditory canal. It's essential to verify coding details and guidelines with the latest resources or coding manuals, as coding practices may change.
* Anal atresia -- congenital absence of a hole at the bottom end of the intestine. Also called imperforate anus. * Aortic atresia -- congenital absence of the normal valvular opening into the aorta. * Biliary atresia -- absence of the major bile ducts. * Choanal atresia -- congenital failure of one or both nasal passages to open. * Esophageal atresia -- a birth defect in which part of esophagus is not hollow. * Intestinal atresia -- obliteration of the hollow of the small intestine, involving the ileum (50% of cases) or the jejunum or duodenum. * Laryngeal atresia -- congenital failure of the laryngeal opening to develop, resulting in partial or total obstruction at or just above or below the glottis. * Pulmonary atresia -- congenital absence of the pulmonary valve opening in the heart. * Tricuspid atresia -- congenital lack of the tricuspid valve opening. * Vaginal atresia -- congenital occlusion of the vagina or subsequence adhesion (sticking together) of the walls of the vagina occluding it.
atresia
atresia
The medical term for this condition is esophageal atresia. It is a congenital condition where the esophagus does not connect to the stomach. This condition requires surgical intervention to repair the connection between the esophagus and stomach.
Congenital lack of the connection between esophagus and stomach; food cannot enter the stomach
atresia
The two most common congenital esophageal abnormalities are esophageal atresia (EA) and tracheoesophageal fistula (TEF).
The frequency of esophageal atresia is estimated to be around 1 in 2,500 to 1 in 4,000 live births. It is a rare congenital condition where the esophagus does not develop properly, leading to a gap that prevents food and liquids from reaching the stomach.
a surgical procedure performed to correct congenital defects of the esophagus (the muscular tube that connects the mouth to the stomach) and the trachea
Pulmonary atresia is a congenital heart defect where the pulmonary valve does not form properly, leading to a blockage of blood flow from the heart to the lungs. This condition can result in low oxygen levels in the blood and may require surgical intervention to improve blood flow to the lungs.
Atresia is a term related to cavities. Atresia is the condition in which a tube is blocked, or absent.
Heart defects (about 25% of affected infants); Gastrointestinal (digestive) anomalies, including malformed anus (rectum) or twisting of the small intestine (about 16%)