Apple Peel Syndrome

Below you will find more information about Apple Peel Syndrome from Medigest. If you believe that you are suffering from any of the symptoms of Apple Peel Syndrome it is important that you obtain an accurate diagnosis from a medical professional to ensure that you obtain the correct medication or treatment for your condition. There are medical conditions that carry similar symptoms associated with Apple Peel Syndrome and therefore the information provided by Medigest is offered as a guideline only and should never be used in preference to seeking professional medical advice. The information relating to Apple Peel Syndrome comes from a third party source and Medigest will not be held liable for any inaccuracies relating to the information shown.


Apple peel syndrome, also known as Jejunal Atresia, is an extremely rare genetic disorder wherein patients are born without a small part of the fold from the stomach membrane connecting the small intestines to the abdomen. This condition occurs in 1 of 270 babies born alive. It is the most common intestinal obstruction found in one third of all babies.


Diagnosis is made through routine prenatal ultrasound.


Babies with Apple Peel Syndrome require surgery after birth, depending on the extent of the disease and location of the atresia.

Symptoms and Signs

When patients are born with a partial absence of this connector, one of the three parts of the small intestine called the ?jejuna? twists around the colon arteries, which causes blockage. As a result, vomiting, constipation and a swollen abdomen may occur.


The exact cause of Apple peel syndrome is unknown. It has been associated with the abnormal development of the bowel during the first trimester of pregnancy. However, pregnant mothers' diet, lifestyle or other factors did not cause or can prevent this condition.

Discuss Apple Peel Syndrome in our forums

Discuss Apple Peel Syndrome with other members of Medigest in our forums.