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  2. Neurofibroma - Wikipedia

    en.wikipedia.org/wiki/Neurofibroma

    A neurofibroma is a benign nerve-sheath tumor in the peripheral nervous system. In 90% of cases, they are found as stand-alone tumors (solitary neurofibroma, solitary nerve sheath tumor[1] or sporadic neurofibroma[1]), while the remainder are found in persons with neurofibromatosis type I (NF1), an autosomal-dominant genetically inherited disease.

  3. Neurofibromatosis type I - Wikipedia

    en.wikipedia.org/wiki/Neurofibromatosis_type_I

    Café au lait spot characteristic of NF1 Diagnostic criteria of neurofibromatosis type I, requiring at least 2 of the mentioned items. [6]The following is a list of conditions and complications associated with NF-1, and, where available, age range of onset and progressive development, occurrence percentage of NF-1 population, method of earliest diagnosis, and treatments and related medical ...

  4. Neurofibromatosis type II - Wikipedia

    en.wikipedia.org/wiki/Neurofibromatosis_type_II

    Neurofibromatosis type II (also known as MISME syndrome – multiple inherited schwannomas, meningiomas, and ependymomas) is a genetic condition that may be inherited or may arise spontaneously, and causes benign tumors of the brain, spinal cord, and peripheral nerves. The types of tumors frequently associated with NF2 include vestibular ...

  5. Neurofibromatosis - Wikipedia

    en.wikipedia.org/wiki/Neurofibromatosis

    Neurofibromatosis (NF) refers to a group of three distinct genetic conditions in which tumors grow in the nervous system. [1] The tumors are non-cancerous (benign) and often involve the skin or surrounding bone. [1] Although symptoms are often mild, each condition presents differently. Neurofibromatosis type I (NF1) is typically characterized ...

  6. Atypical teratoid rhabdoid tumor - Wikipedia

    en.wikipedia.org/wiki/Atypical_teratoid_rhabdoid...

    A retrospective survey from 36 AT/RT cases at St. Jude Children's Hospital from 1984 to 2003 showed that the two-year event-free survival (EFS) for children under three was 11%, and the overall survival (OS) rate was 17%. For children aged 3 years or older, the EFS was 78% and the OS 89%. [6]

  7. Selumetinib - Wikipedia

    en.wikipedia.org/wiki/Selumetinib

    Key:CYOHGALHFOKKQC-UHFFFAOYSA-N Y. (verify) Selumetinib (INN), [13] sold under the brand name Koselugo, is a medication for the treatment of children, two years of age and older, with neurofibromatosis type I (NF-1), a genetic disorder of the nervous system causing tumors to grow on nerves. [14] It is taken by mouth.

  8. Why Milton could become one of the most destructive ...

    www.aol.com/life-threatening-storm-surge-likely...

    The metropolitan area is home to more than 3 million residents. “Milton has the potential to be one of the most destructive hurricanes on record for west-central Florida,” the National ...

  9. Neurofibromin - Wikipedia

    en.wikipedia.org/wiki/Neurofibromin

    NF1 was cloned in 1990 [11][12] and its product neurofibromin was identified in 1992. [13][14][15][16] Neurofibromin, a GTPase-activating protein, primarily regulates the protein Ras. [17] NF1 is located on the long arm of chromosome 17, position q11.2 [7] NF1 spans over 350- kb of genomic DNA and contains 62 exons.