Hirschsprug's Disease is a congenital condition in which nerve cells (ganglia) are missing from segments of the colon. Without these nerves, the bowel can't coordinate muscle contractions to move stool along, leading to blockage and severe constipation. It typically presents in newborns but milder cases may not be diagnosed until later in childhood or adulthood. (ICD-10 code: Q43.1)
Symptoms vary depending on age and the length of bowel involved. Common signs include:
Hirschsprug's Disease is primarily driven by genetic factors. Known contributors include:
At GastroDoxs in Jersey Village, we specialize in diagnosing and treating Hirschsprung's Disease for patients of all ages. Our multidisciplinary team offers precise ICD-10 coding (Q43.1), advanced pull-through surgeries and tailored bowel management programs. We combine cutting-edge techniques with compassionate, patient-centered care to ensure the best possible outcomes. Don't wait-take the first step toward relief today.
Book an Appointment Now: Call us at 832-632-4070 or visit our website to schedule your consultation with a Hirschsprung's Disease specialist in Jersey Village.
We've successfully treated more than 1K patients, helping individuals improve their digestive health and overall well-being through expert, personalized care.
With over 20 years of experience, GastroDoxs has been a trusted provider of gastroenterology care, focusing on delivering the best outcomes for patients
Dr. Bharat Pothuri is a Board-Certified Gastroenterologist and Hepatologist. With extensive experience in digestive health, he specializes in advanced endoscopic procedures, chronic GI disorder management, and preventive care. Dr. Pothuri is dedicated to providing expert, patient-focused insights to help improve gut health and overall well-being.
The ICD-10 code for Hirschsprug's Disease is Q43.1, used for accurate billing and medical records.
Yes. While it's often diagnosed at birth, milder forms may present in teens or adults, usually manifesting as chronic constipation.
Hirschsprug's Disease is primarily genetic, often linked to mutations in the RET gene and a family history of bowel issues. Rarely, it's associated with syndromes like Down syndrome.
Diagnosis typically involves a contrast enema to visualize the colon, a rectal biopsy to check for nerve cells, and anorectal manometry to assess muscle function.
In newborns, key signs include failure to pass meconium within 48 hours, abdominal distension, vomiting, and feeding difficulties.
Treatment focuses on restoring bowel function. Surgical options include pull-through procedures (Swenson, Soave, Duhamel) to remove the affected segment. Non-surgical bowel management with diet modifications and laxatives may also be used.
Consult a specialist if your newborn hasn't passed stool in two days, or if you or your child experience chronic constipation, abdominal pain, or bloating.
Most patients require pull-through surgery to remove the nerve-lacking colon. The specific timing and surgical approach depend on disease severity and individual factors.
Hospital stays usually last 5-7 days. Full return of bowel function can take weeks to months, and follow-up care ensures optimal recovery.
Call GastroDoxs to schedule an appointment or search online for "Hirschsprug's Disease specialist near Jersey Village" to connect with our experts.
