The Hirschsprug Disease is a congenital disorder where nerve cells (ganglia) are absent in parts of the colon. In their absence, the bowel is unable to create muscle contractions to drag the stool along and become blocked, thus causing acute constipation. It usually occurs in newborns but the milder forms could not be diagnosed until further on during childhood or adulthood. (ICD-10 code: Q43.1)
However, the symptoms change depending on age and the bowel involved. Common signs include:
The disease of Hirschsprug is mostly genetic. Known contributors include:
In Jersey Village, GastroDoxs is the place where all patients can get diagnosed and treated with Hirschsprung Disease. ICD-10 (Q43.1) coding is obtained by our multidisciplinary team, in addition to advanced analysis of pull-through surgery and personalized bowel management programs. Our highly advanced methods are accompanied by patient-focused care and compassion to achieve the most desirable results. Wait-do not wait any more days.
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.
Hirschsprug Disease ICD-10 code Q43.1 is appropriate to bill and keep medical records.
Yes. Although it is usually diagnosed later, at birth, more mild cases of the condition can be replicated in teens or adults, most of the time as chronic constipation.
The Disease is mostly hereditary, it is actively manifested when an individual has defects in the RET gene and a bowel malfunction in the family history. Seldom, it is correlated with such syndromes as Down syndrome.
Diagnosis normally includes contrast enema to view the colon, a rectal biopsy to examine the presence of nerve cells and anorectal manometry to determine muscle activity.
Passing meconium in newborns during the 48 hours following delivery: failure to pass these in newborns is one of the primary signs of necrotizing intensive care. Additionally, there are signs of abdominal distension, vomiting, and difficulty feeding in the newborn.
The treatment is aimed at regaining bowel movement. Surgical correction can be done by using pull-through procedures (Swenson, Soave, Duhamel) to excise the segment that is affected. Surgical bowel management may also be employed as dietary and laxative modifications.
See a specialist in case your newborn has never stooled within two days or in case of chronic constipation, belly pains, and bloating of the abdomen of you or your child.
Majority of patients need the pull-through surgery procedure in order to extract the colon with no nerve. Surgery and when to practice it are determined by the severity of the diseases and personal considerations.
The duration of hospital stay is most of the times 5-7 days. It can take weeks to months before full recovery of bowel functions and post-discharge care can ensure the best recovery.
To contact our professionals, call GastroDoxs and make an appointment or use the Internet and find the specialist in Hirschspurg disease around the Jersey Village.
