An infant born with this defect will at first appear all right, swallowing normally. However, the blind pouch will begin to fill with mucus and saliva that would normally pass through the esophagus to the stomach. These secretions back up.
* 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.
Pulmonary Atresia (or Pulmonary Stenosis) Right Ventricular Hypertrophy Ventricular Septal Defect Overriding Aorta
used to investigate the extent defect in the anal or rectal atresia. The anus is marked with radio opaque marker, the baby is inverted. A lateral radio graph is taken in the air, the rectum will rise to the highest point, giving an indication of the extent of the atresia.
The specific cause of this birth defect is unknown, so all that women can do is to practice the many general preventive measures, even before they conceive.
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.
Esophageal atresia is typically diagnosed shortly after birth when a baby has trouble swallowing, excessive drooling, and choking when feeding. Diagnostic tests such as a chest X-ray, contrast dye study (esophagram), and/or endoscopy may be performed to confirm the diagnosis and determine the severity of the condition.
This defect may cause children to develop an accumulation of cerebrospinal fluid on the brain (hydrocephalus ).
About half of the population is born with genetic defects....1/3 of us dont know it..
Both male and female children have gotten this birth defect.
As long as the 'health defect' isn't a communicable disease - there's absolutely no reason why not !
Would you rather have a Homicidal, Sociopathic Serial Rapist terrorizing your children?