VHL syndrome (von Hippel-Lindau syndrome)

VHL syndrome (von Hippel-Lindau syndrome) is a genetic condition caused by a mutation in the VHL gene, leading to abnormal growths or tumors in various organs, including the eyes, brain, spinal cord, kidneys, and pancreas. These tumors can be benign or cancerous, and their development varies among individuals. Since it’s inherited, family members may also carry the gene mutation. Early detection and regular monitoring are crucial for managing risks, and treatment may involve surgery, medication, or other therapies to address tumors and prevent complications.