Congenital aganglionosis of the distal bowel defines Haddad syndrome.
Aganglionosis begins with the anus, which is always involved, and continues proximally or upwards for a variable distance.
Both the myenteric (Auerbach) plexus and the submucosal (Meissner) plexus are absent, resulting in reduced bowel peristalsis and function.
Haddad syndrome is associated with
Approximately 10% of patients with Haddad syndrome have a positive family history
Haddad syndrome occurs more often in males than in females, with a male-to-female ratio of approximately 4:1.
Management of complications of unrecognized or untreated Haddad syndrome
Colonic lavage may also need to be used in postoperative patients who develop enterocolitis as a complication.
Treatment of Haddad syndrome consists of surgical resection of the abnormal section of the colon, followed by reanastomosis
Common surgical procedure- Swenson and Duhamel surgery