Neurofibromatosis Signs and symptoms
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(benign) and often involve the skin or surrounding bone. Although symptoms are often mild, each condition presents differently. Neurofibromatosis type I...
Neurofibromatosis type I (NF-1), or von Recklinghausen syndrome, is a complex multi-system human disorder caused by the mutation of neurofibromin 1 (NF-1)...
Neurofibromatosis type II (also known as MISME syndrome – multiple inherited schwannomas, meningiomas, and ependymomas) is a genetic condition that may...
Legius syndrome (redirect from Neurofibromatosis type 1-like syndrome)in 2007 and is often mistaken for neurofibromatosis type I. It is caused by mutations in the SPRED1 gene. It is also known as neurofibromatosis type 1-like...- Familial multiple cafe-au-lait spots (redirect from Neurofibromatosis type 6)characteristic tell-tale sign of neurofibromatosis, multiple cafe au lait spots; however, testing of the gene usually involved in neurofibromatosis revealed it to...
Scoliosis (section Signs and symptoms)such as muscle spasms, cerebral palsy, Marfan syndrome, and tumors such as neurofibromatosis. Diagnosis is confirmed with X-rays. Scoliosis is typically...
epiphyseal dysplasia, Al-Gazali type Myhre syndrome Neurofibromatosis, type 1 Neurofibromatosis-Noonan syndrome Niemann-Pick disease, type A Noonan syndrome...
Glioblastoma (section Signs and symptoms)headaches, personality changes, nausea, and symptoms similar to those of a stroke. Symptoms often worsen rapidly and may progress to unconsciousness. The...
Meningioma (section Signs and symptoms)medical imaging. If there are no symptoms, periodic observation may be all that is required. Most cases that result in symptoms can be cured by surgery. Following...
Dural ectasia (section Signs and symptoms)syndrome. It may also occur in Ehlers-Danlos Syndrome, neurofibromatosis type I, ankylosing spondylitis, and is associated with spondylolisthesis, vertebral...
Chiari malformation (redirect from Chiari symptom)terms of size and extent of symptoms actually stays stable throughout a lifetime. Syringomyelia symptoms include pain, weakness, numbness, and stiffness in...
Brain tumor (section Signs and symptoms)greatest of any type of cancer. The signs and symptoms of brain tumors are broad. People may experience symptoms regardless of whether the tumor is benign...
Proteus syndrome (section Signs and symptoms)glypican 3 and may play a role in regulating cell division and growth regulation. Macrodystrophia lipomatosa Fibrolipomatous hamartoma Neurofibromatosis type...
Non-ossifying fibroma (section Signs and symptoms)occur in neurofibromatosis, or Jaffe–Campanacci syndrome in combination with cafe-au-lait spots, mental retardation, hypogonadism, eye and cardiovascular...- physical characteristic common to patients with tuberous sclerosis and neurofibromatosis that he examined. The term phakomatoses was derived from phakos...
Angiosarcoma (category Dermal and subcutaneous growths)radiation therapy, neurofibromatosis, Maffucci syndrome, Klippel-Trenaunay syndrome and chemicals such as arsenic, thorotrast and vinyl chloride. A 2020...- Spinal tumor (section Signs and symptoms)lung, and kidney cancer. There are many genetic factors associated with intradural tumors, most commonly neurofibromatosis 1 (NF1), neurofibromatosis 2 (NF2)...
Macroglossia (section Signs and symptoms)be asymptomatic, symptoms usually are more likely to be present and more severe with larger tongue enlargements. Signs and symptoms include: Dyspnea –...- cause signs and symptoms secondary to compression of nearby cranial nerves, including cranial nerve V (trigeminal), cranial nerve VII (facial), and cranial...
- annual Neurofibromatosis Prize for Research Ideas competition, sponsored by National Neurofibromatosis Foundation and the International Neurofibromatosis Association...
- hypoventilation syndrome (G47.35) familial dysautonomia [Riley-Day] (G90.1) neurofibromatosis (nonmalignant) (Q85.0) Q07.0 Arnold-Chiari syndrome Arnold-Chiari
- GeneReviews. "Neurofibromatosis 2" (2002). "Neurofibromatosis Type 2: Information for Patients and Families." National Neurofibromatosis Foundation brochure