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  2. Neurofibromatosis - Wikipedia

    en.wikipedia.org/wiki/Neurofibromatosis

    Life long [1] Types: Neurofibromatosis type 1 (NF1), neurofibromatosis type 2 (NF2), schwannomatosis [1] Causes: Genetic [1] Diagnostic method: Symptoms, genetic testing [2] Treatment: Surgery, radiation therapy [2] Prognosis: NF1: variable, but most of the time normal life expectancy [1] NF2: shortened life expectancy [1] Frequency: 1 in 3,000 ...

  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. List of countries by life expectancy - Wikipedia

    en.wikipedia.org/wiki/List_of_countries_by_life...

    UN: Estimate of life expectancy for various ages in 2023; Locations Life expectancy for population in general Life expectancy for male Life expectancy for female Sex gap; at birth bonus 0→15 at 15 bonus 15→65 at 65 bonus 65→80 at 80 at birth at 15 at 65 at 80 at birth at 15 at 65 at 80 at birth at 15 at 65 at 80 Hong Kong: 85.51: 0.21: 70 ...

  6. Malignant peripheral nerve sheath tumor - Wikipedia

    en.wikipedia.org/wiki/Malignant_peripheral_nerve...

    A malignant peripheral nerve sheath tumor is rare, but is one of the most common frequent soft tissue sarcoma in the pediatric population. About half of these cases also happen to occur along with neurofibromatosis type 1 (NF-1), which is a genetic mutation on the 17th chromosome which causes tumors along the nervous system.

  7. Moyamoya disease - Wikipedia

    en.wikipedia.org/wiki/Moyamoya_disease

    Moyamoya disease is a disease in which certain arteries in the brain are constricted. Blood flow is blocked by constriction and blood clots (). [2]A collateral circulation develops around the blocked vessels to compensate for the blockage, but the collateral vessels are small, weak, and prone to bleeding, aneurysm and thrombosis.

  8. Legius syndrome - Wikipedia

    en.wikipedia.org/wiki/Legius_syndrome

    CHR 15. Legius syndrome is a phakomatosis [8] and a RASopathy, a developmental syndrome due to germline mutations in genes. [7] [9] The condition is autosomal dominant in regards to inheritance and caused by mutations to the SPRED1 gene at chromosome 15, specifically 15q14 (or (GRCh38): 15:38,252,086-38,357,248).

  9. Schwannomatosis - Wikipedia

    en.wikipedia.org/wiki/Schwannomatosis

    Schwannomatosis is an extremely rare genetic disorder closely related to the more-common disorder neurofibromatosis (NF). Originally described in Japanese patients, [1] it consists of multiple cutaneous schwannomas, central nervous system tumors, and other neurological complications, excluding hallmark signs of NF. The exact frequency of ...

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