What is Familial Pancreatic Cancer?
What is familial GIST?
ON THIS PAGE: You will find some basic information about this disease and the parts of the body it may affect. This is the first page of Cancer.Net’s Guide to Eyelid Cancer. To see other pages, use the menu on the side of your screen. Think of that menu as a roadmap to this full guide.
What is Werner syndrome?
What is xeroderma pigmentosum?
Xeroderma pigmentosum (XP) is a hereditary condition characterized by extreme sun sensitivity, leading to a very high risk of skin cancer. Eye problems are also common. Neurologic problems—including learning disabilities, progressive hearing loss, progressive neuromuscular degeneration, loss of some reflexes, and occasionally, tumors in the central nervous system—occur in some people with XP.
What is tuberous sclerosis complex?
Tuberous sclerosis complex (TSC) is a hereditary condition associated with changes in the skin, brain, kidney, and heart. Seizures are a frequent complication, and some people with TSC have learning disabilities.
What is Peutz-Jeghers syndrome?
What is Nevoid Basal Cell Carcinoma Syndrome?
What is neurofibromatosis type 2?
Neurofibromatosis type 2 (NF2) is a hereditary condition most commonly associated with bilateral vestibular schwannomas, also known as acoustic neuromas. These are benign (noncancerous) tumors that occur on the nerves for balance leading to the inner ear. Although these tumors are benign, they can cause hearing and balance problems.