atresia
Congenital lack of the connection between esophagus and stomach; food cannot enter the stomach
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.
Ametria is the congenital lack of a uterus.
No, humans and most animals have one esophagus. Having two esophaguses would be a rare congenital condition known as double esophagus or duplicated esophagus, where the individual has two separate and functional esophagi.
In the business world we are running like a horse. In this we face every thing and do so many thing for reach the particular goal in the same we miss something for negligence or careless of the particular thing, so lack of continuity will arise for the negligence.
Yes, cretinism is the condition caused by congenital lack of thyroid secretion. Neonatal thyroid testing is an important preventive strategy. Cretinism can be prevented by thyroid supplementation in patients with congenital hypothyroidism.
Arrested physical and mental development resulting from a congenital lack of thyroid secretion is known as Cretinism.
The two most common congenital esophageal abnormalities are esophageal atresia (EA) and tracheoesophageal fistula (TEF).
Narrowing in the esophagus, known as esophageal stricture, can occur in several locations, most commonly at the lower esophagus due to gastroesophageal reflux disease (GERD) or at the upper esophagus due to conditions like achalasia. It can also occur at the mid-esophagus, often due to tumors, inflammation, or scarring from injury or surgery. Additionally, congenital factors can lead to narrowing in various regions throughout the esophagus.
a surgical procedure performed to correct congenital defects of the esophagus (the muscular tube that connects the mouth to the stomach) and the trachea
Albino is a term that means a rare congenital condition that causes total lack of pigmentation in the body.
Surgery is recommended for congenital heart defects that result in a lack of oxygen, a poor quality of life, or a patient who does not thrive.