📂 Diseases
Hirschsprung disease-ganglioneuroblastoma syndrome — Definition
Hirschsprung hastalığı-ganglionöroblastom sendromu / Hirschsprung disease-ganglioneuroblastoma syndrome
Hirschsprung disease and ganglionöroblastomun are a rare genetic syndrome. Hirschsprung disease is characterized by disruption of intestinal movements due to the absence of nerve cells (ganglion cells). Ganglionöroblastom is a tumor caused by the sympathetic nervous system and is often benign dilut. This syndrome is associated with mutations in the RET gene and shows autosomal dominant inheritance.
Frequently Asked Questions
❓ What is Hirschsprung hastalığı-ganglionöroblastom sendromu?
Hirschsprung hastalığı-ganglionöroblastom sendromu; hirschsprung disease and ganglionöroblastomun are a rare genetic syndrome. Hirschsprung disease is characterized by disruption of intestinal movements due to the absence of nerve cells (ganglion cells). Ganglionöroblastom is a tumor caused by the sympathetic nervous system and is often benign dilut. This syndrome is associated with mutations in the RET gene and shows autosomal dominant inheritance.
❓ What is Hirschsprung disease-ganglioneuroblastoma syndrome in Turkish?
The Turkish equivalent of "Hirschsprung disease-ganglioneuroblastoma syndrome" is Hirschsprung hastalığı-ganglionöroblastom sendromu.
❓ Which medical field is Hirschsprung hastalığı-ganglionöroblastom sendromu related to?
This term belongs to the Diseases category.