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Contingency for Novel Diagnosis and Therapies for Hirschsprung’s Disease

1, 1, 2, 3

  1. 1Department of Pharmaceutics, Dayanand Education Society, Dayanand College of Pharmacy, Latur, Maharashtra, INDIA..
  2. 2Department of Pharmaceutical Quality Assurance, Dayanand Education Society, Dayanand College of Pharmacy, Latur, Maharashtra, INDIA..
  3. 3Department of Pharmacognosy, Dayanand Education Society, Dayanand College of Pharmacy, Latur, Maharashtra, INDIA..

CORRESPONDENCE

Sayali Arun Dongare

Department of Pharmaceutics, Dayanand Education Society, Dayanand College of Pharmacy, Latur, Maharashtra, INDIA..

sayali1622002@gmail.com

Received: 11-11-2024; Accepted: 20-01-2025.

Volume 18, Issue 3 · pp. 257-261 · 2025 · DOI: 10.5530/ijopp.20250219

ABSTRACT

The majority of frequent reason of low functional blockage of the bowel in pediatrics is a Hirschsprung disease, which is brought on by a genetic mutation that disrupts the enteric nerve system. The absence of enteric ganglia over a varied length of intestine characterizes this developmental condition, which is classified as a neurocristopathy. Hirschsprung disease is a complicated surgical and medical condition that seems to have different social and health consequences based on the age of the patient and level of neurodevelopment. This review examines the genetic variables that influence development of Hirschsprung disease as well as its prevalence and congenital connection. An overview of a Hirschsprung's disease and its etiology, diagnosis, course of therapy are the goals of this article.

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    Dongare, S. A., Bastapure, R. S., Lohiya, G. V., & Satpute, K. L. (2025). Contingency for Novel Diagnosis and Therapies for Hirschsprung’s Disease. Indian Journal of Pharmacy Practice, 18(3), 257-261. https://doi.org/10.5530/ijopp.20250219

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    © 2025 Author(s)

    This is an open access article distributed under the terms of the Creative Commons Attribution 4.0 License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. CC BY 4.0