Neurofibromitosis Program

Neurofibromatosis I, a genetic disorder involving neural tissues, may include symptoms such as multiple hyperpigmented areas (cafe-au-lait spots), pseudarthroses (false joint), scoliosis, tumors, or raised lumps anywhere on the body. Cosmetic disorders may be a problem, as well as language and learning disabilities. The Neurofibromatosis Program is multidisciplinary, including the expertise of specialists in Developmental Pediatrics, Genetics, Neurology, Orthopedics, and Psychology, with other medical, mental health, and ancillary services available. This program meets the staffing and clinical genetic consulting parameters set by the National Neurofibromatosis Foundation and Neurofibromatosis, Inc. Adult patients with this disorder are referred to local specialists in Delaware, to the adult genetics clinic at the University of Pennsylvania, or to other physicians and facilities. Neurofibromatosis II is usually a disease with adult onset and new patients over 18 cannot be seen.