UN ANÁLISIS EN PROFUNDIDAD DE LA ENFERMEDAD DE HIRSCHSPRUNG. COMPRENSIÓN DE LA FISIOPATOLOGÍA, ENFOQUES DE DIAGNÓSTICO Y TRATAMIENTO.

Hirschsprung disease (HD), a congenital disorder characterized by the absence of ganglion cells in the intestines, presents a complex interplay of genetic, molecular, and clinical factors that significantly affect patient outcomes. As research continues, emerging therapies and innovative approaches show promise in improving treatment effectiveness and quality of life for affected individuals. This article seeks to provide an in-depth analysis of Hirschsprung disease, exploring its intricate pathophysiology, diagnostic methodologies and evolving treatment strategies, thereby contributing to a comprehensive understanding of this complex condition and its implications for clinical practice.