ARITURK, ETOSYALI, NARITURK, N2024-04-242024-04-2419920041-4301https://hdl.handle.net/11468/22189Waardenburg's syndrome is characterized by a broad nasal root, pigmentation disturbance and congenital deafness while aganglionosis is described as the partial or complete lack of ganglion cells in the alimentary tract. This report describes a five-day-old male infant with Waardenburg's Syndrome associated with total aganglionosis of the colon, ileum and distal jejunum and draws attention to the causal relationship between these two entities.eninfo:eu-repo/semantics/closedAccessWaardenburg SyndromeHirschsprungs DiseaseNeural CrestA CASE OF WAARDENBURG SYNDROME AND AGANGLIONOSISA CASE OF WAARDENBURG SYNDROME AND AGANGLIONOSISArticle342111114WOS:A1992JL486000081440950N/A