Neurofibromatosis type II (also known as MISME syndrome – multiple inherited schwannomas, meningiomas, and ependymomas) is a genetic condition that may...
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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...
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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)...
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along with his brothers and mother. He has a genetic condition, neurofibromatosis type II. He is also the founder and CEO of Chakriwat Medical Information...
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JDBC type 2 driver Kawanishi H8K, Type 2 flying boat (code named Emily) Motorola Type II Multiple endocrine neoplasia type 2 Neurofibromatosis type II R-Type...
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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...
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ABIs have been used in children and adults, and in patients with neurofibromatosis type II. The auditory brainstem implant was first developed in 1979 by...
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Phakomatosis (section Neurofibromatosis Type II)
neurofibromatosis type 1. Epilepsy is seen in 4-7% of patients. Musculoskeletal system manifestations can develop in patients with neurofibromatosis type...
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considered to be the hallmark and main diagnostic criterion of Neurofibromatosis Type II (NF2), a genetic disorder that is heritable, progressive, difficult...
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can be caused by an ependymoma. Ependymomas are also seen with neurofibromatosis type II. Source: severe headache visual loss (due to papilledema) vomiting...
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protein. In humans, it is a tumor suppressor protein involved in neurofibromatosis type II. Sequence data reveal its similarity to the ERM protein family...
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syndrome Prader–Willi syndrome Angelman syndrome Neurofibromatosis type I Neurofibromatosis type II Williams syndrome Miller–Dieker syndrome Smith–Magenis...
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aircraft Nickel & Foucard NF-2 Asterix, a French homebuilt aircraft Neurofibromatosis type II, an inherited disease Merlin (protein) or Neurofibromin 2, a cytoskeletal...
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Neurofibroma (section Types)
sporadic neurofibroma), while the remainder are found in persons with neurofibromatosis type I (NF1), an autosomal-dominant genetically inherited disease. They...
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The following is a list of genetic disorders and if known, type of mutation and for the chromosome involved. Although the parlance "disease-causing gene"...
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different proteins: Neurofibromin 1 Neurofibromin 2 Neurofibromatosis type I Neurofibromatosis type II This disambiguation page lists articles associated...
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John Henry Wishart gives the first description in England of neurofibromatosis type II. Navier–Stokes equations in fluid dynamics first formulated. May...
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correlation between autism and developmental delay in general. Neurofibromatosis type II occurs in a significant minority of cases of ring chromosome 22...
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Macrocephaly (redirect from Macrocephaly dominant type)
the holgate gene, autism, PTEN mutations such as Cowden disease, neurofibromatosis type 1, and tuberous sclerosis; overgrowth syndromes such as Sotos syndrome...
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patients. Children with certain hereditary diseases, such as neurofibromatosis type II (NF2), have been found to be more frequently afflicted with this...
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about 2% of orbital tumors, and about 10% of optic nerve lesions. Neurofibromatosis type II (NF-2) affects around 9% of ONSM patients, where the incidence...
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Chiari malformation (redirect from Chiari type 2)
malformations include X-linked vitamin D-resistant rickets, and neurofibromatosis type I.[citation needed] Diagnosis is made through a combination of patient...
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alter cellular growth control, and neural development, resulting in neurofibromatosis type 1 (NF1, also known as von Recklinghausen syndrome). Symptoms of...
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50% of cases, with marfanoid habitus and with mucosal and digestive neurofibromatosis.[citation needed] In familial isolated medullary thyroid carcinoma...
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his activist art. Ed Port was diagnosed at the age of 3 with neurofibromatosis type II, which caused a growing tumor on his face. The growth of the tumor...
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Neurofibromatosis Neurofibromatosis type 2 Neurofibromatosis type 3 Neurofibromatosis type 6 Neurofibromatosis, familial intestinal Neurofibromatosis...
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history of the condition, and neurofibromatosis type 2. They appear to be able to form from a number of different types of cells including arachnoid cells...
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not known. Uncommon risk factors include genetic disorders, such as neurofibromatosis and Li–Fraumeni syndrome, and previous radiation therapy. Glioblastomas...
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Noonan syndrome with multiple lentigines (redirect from Gorlin syndrome type II)
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);...
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Alcino J. Silva (section Development of treatments for cognitive deficits in neurofibromatosis type I and tuberous sclerosis)
1996 VW Foundation, 1996 Neurofibromatosis Consortium, 1996 Neurofibromatosis Foundation, 1996 Perkin Fund, 1997 Neurofibromatosis Foundation, 1997 National...
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