Anorectal Malformation
What is Anorectal Malformation?
Anorectal Malformation (ARM) is a congenital condition where the opening of the anus and rectum is abnormally developed. It can occur in varying degrees — from a simple narrowing of the anal opening to a complete absence of the anal opening or abnormal connection with the urinary or reproductive system. Early diagnosis and timely surgical intervention are crucial for a healthy outcome.
Symptoms of Anorectal Malformation
- Absence of anal opening at birth
- Abdominal swelling or distension
- Inability to pass stool normally
- Passing stool through the urinary tract or vagina (in some cases)
- Constipation or bowel control issues
Diagnosis
Diagnosis is usually made soon after birth through physical examination and imaging tests such as:
- Ultrasound
- X-ray
- MRI or CT Scan
Treatment Options
The primary treatment for anorectal malformation is corrective surgery, which may include:
- Anoplasty - Creating a proper anal opening.
- Posterior Sagittal Anorectoplasty (PSARP) - Reconstruction of the rectum and anal canal to restore normal anatomy.
- Colostomy - Temporary diversion of stool in complex cases, followed by corrective surgery later.
Why Choose Us for ARM Treatment?
- Experienced pediatric and colorectal surgeons
- Advanced surgical techniques for better outcomes
- Comprehensive post-operative care
- Child-friendly environment and compassionate care
Early detection and expert treatment can help your child lead a healthy and normal life. If your child is diagnosed with an anorectal malformation, consult our specialized surgical team today for a detailed evaluation and treatment plan.
