Neurofibromatosis Epidemiology
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Figure of various morbidities associated with neurofibromatosis type II. The three types of neurofibromatosis are caused by different mutations on chromosomes...
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)...
is considered to be the hallmark and main diagnostic criterion of Neurofibromatosis Type II (NF2), a genetic disorder that is heritable, progressive,...
Genetic disorder (section Epidemiology)this type of disorder are Huntington's disease,: 58 neurofibromatosis type 1, neurofibromatosis type 2, Marfan syndrome, hereditary nonpolyposis colorectal...
Meningioma (section Epidemiology)during radiation therapy, a family history of the condition, and neurofibromatosis type 2. They appear to be able to form from a number of different...
Glioblastoma (section Epidemiology)not known. Uncommon risk factors include genetic disorders, such as neurofibromatosis and Li–Fraumeni syndrome, and previous radiation therapy. Glioblastomas...
Scoliosis (section Epidemiology)muscle spasms, cerebral palsy, Marfan syndrome, and tumors such as neurofibromatosis. Diagnosis is confirmed with X-rays. Scoliosis is typically classified...
Sarcoma (section Epidemiology)including Li-Fraumeni syndrome, familial adenomatous polyposis, neurofibromatosis type 1, and heritable RB1 gene mutations. Kaposi sarcoma is caused...
Noonan syndrome is fairly common (1:1,000 to 1:2,500 live births), and neurofibromatosis 1 (which was once thought to be related to NSML) is also common (1:3500);...
surgical removal is often successful. Schwannomas can be associated with neurofibromatosis type II, which may be due to a loss-of-function mutation in the protein...
Osteitis fibrosa cystica (section Epidemiology)disease of bone (not to be confused with von Recklinghausen's disease, neurofibromatosis type I), is caused by hyperparathyroidism, which is a surplus of parathyroid...
Angiosarcoma (section Epidemiology)needed] Accepted risk factors include lymphedema, radiation therapy, neurofibromatosis, Maffucci syndrome, Klippel-Trenaunay syndrome and chemicals such...
Brain tumor (section Epidemiology)Epstein–Barr virus, ionizing radiation, and inherited syndromes such as neurofibromatosis, tuberous sclerosis, and von Hippel-Lindau Disease. Studies on mobile...
Winged scapula (section Epidemiology)may be useful to rule out certain diagnoses if suspected, such as neurofibromatosis-related injury, intervertebral disc disorder, radiculopathy, and tumors...
Intracranial aneurysm (section Epidemiology)aneurysms. This includes: autosomal dominant polycystic kidney disease, neurofibromatosis type I, Marfan syndrome, multiple endocrine neoplasia type I, pseudoxanthoma...
Macroglossia (section Epidemiology)hypothyroid disorders. Other causes include mucopolysaccharidosis, neurofibromatosis, multiple endocrine neoplasia type 2B, myxedema, acromegaly, angioedema...
Inflammatory fibroid polyp (section Epidemiology)granular cell tumors and certain immune system conditions, such as neurofibromatosis, Crohn's disease, ankylosing spondylitis, and human immunodeficiency...
Neuroblastoma (section Epidemiology)familial neuroblastoma, as well. Neuroblastoma is also a feature of neurofibromatosis type 1 and the Beckwith-Wiedemann syndrome. MYCN oncogene amplification...
hereditary predisposition. The main hereditary predispositions are mainly neurofibromatosis type I, Li-Fraumeni syndrome, hereditary nonpolyposis colorectal cancer...
Megalencephaly (section Epidemiology)Prasanna D (January 2014). "Cranio-orbital-temporal neurofibromatosis: an uncommon subtype of neurofibromatosis type-1". Oman Journal of Ophthalmology. 7 (1):...
- children <20 years, 75% in <10 year olds; 10% in adults Associated with neurofibromatosis 30% of OPG patients have NF1 stigmata Up to 25% of NF1 patients develop