Lindau Disease
Also written as VHL.
Deafness and\nfacial weakness may result from the operation.\nVon Hippel–Lindau disease\nThis is a dominantly inherited disease characterised by the combina tion of retinal and intracranial (typically cerebellar) haemangiomas\nand haemangioblastomas.
What our notes say
- Deafness and\nfacial weakness may result from the operation.\nVon Hippel–Lindau disease\nThis is a dominantly inherited disease characterised by the combina tion of retinal and intracranial (typically cerebellar) haemangiomas\nand haemangioblastomas. (Davidson's Essentials of Medicine - 2nd)
- Cystic lesions of the kidneys, pancreas, liver, and epididymis, as well as pheochromocytoma, are frequently associated with von Hippel–Lindau disease. (Neurocutaenous syndromes)
- \nVON HIPPEL-LINDAU DISEASE\nThis is a rare autosomal dominant inherited disorder\ncharacterised by haemangiomatous cystic lesions in the\nretina and cerebellum, sometime also in spinal cord,\nkidney, liver and pancreas. (Devendra K. Gupta, Krishna M. Goel - Hutchison’s Paediatrics. chdhe-Jaypee Broth)
- Verapamil von Hippel-Lindau disease ischemic heart disease, 398\nfor accessory pathway-mediated clinical features of, 456t\ntachycardia, 167 genetic factors in, 456t Xanthoma, palmar crease, 64\nadverse effects of, 399t VSD. (Harrisons Cardiovascular Medicine 2nd Edition 2)
- Von Hippel-Lindau disease 381 oedema 695f Yolk sac tumour recurrence 276f (Devendra K. Gupta, Krishna M. Goel - Hutchison’s Paediatrics. chdhe-Jaypee Broth)
- Association: Von Hippel-Lindau disease — cerebellar, brain stem, retinal, pancreatic, and hepatic cavernous hemangiomas (VASCULAR PATHOLOGY — Must-Know Comprehensive Notes — Notes)
Study material on Lindau Disease
- Neurocutaenous syndromes
- Neurocutaenous syndromes
- Harrisons Cardiovascular Medicine 2nd Edition 2
- Devendra K. Gupta, Krishna M. Goel - Hutchison’s Paediatrics. chdhe-Jaypee Brothers (2012)