Hirschsprung's disease in a genetically diagnosed Cri-du-chat syndrome baby

• Prif Awduron: Mohammad Aldaffaa (Awdur), Arwa Mahfouz (Awdur), Suliaman Alaqeel (Awdur), Hajar Abdullah Alakeel (Awdur), Mohammed Al Naamshan (Awdur)
• Fformat: Llyfr
• Cyhoeddwyd: Elsevier, 2023-04-01T00:00:00Z.
• Pynciau: article
• Mynediad Ar-lein: Connect to this object online.

Introduction: Hirschsprung's disease (HSD) is a congenital disease characterized by the absence of ganglion cells in the myenteric and submucosal plexuses of the gastrointestinal tract. Many genetic causes of HSD have been investigated, although the most common and widely accepted is the RET ge...