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  2. Chronic lymphocytic leukemia - Wikipedia

    en.wikipedia.org/wiki/Chronic_lymphocytic_leukemia

    904,000 (2015) [6] Deaths. 60,700 (2015) [7] Chronic lymphocytic leukemia (CLL) is a type of cancer in which the bone marrow makes too many lymphocytes (a type of white blood cell). [2][8] Early on, there are typically no symptoms. [2] Later, non-painful lymph node swelling, feeling tired, fever, night sweats, or weight loss for no clear reason ...

  3. Cerebellar degeneration - Wikipedia

    en.wikipedia.org/wiki/Cerebellar_degeneration

    It is located above the brain stem, posterior to the brain. Cerebellar degeneration is a condition in which cerebellar cells, otherwise known as neurons, become damaged and progressively weaken in the cerebellum. [1] There are two types of cerebellar degeneration; paraneoplastic cerebellar degeneration, and alcoholic or nutritional cerebellar ...

  4. Gerstmann–Sträussler–Scheinker syndrome - Wikipedia

    en.wikipedia.org/wiki/Gerstmann–Sträussler...

    Gerstmann–Sträussler–Scheinker syndrome. A person with inherited prion disease has cerebellar atrophy. This is quite typical of GSS. difficulty speaking, developing dementia, memory loss, vision loss. Gerstmann–Sträussler–Scheinker syndrome (GSS) is an extremely rare, always fatal (due to it being caused by prions) neurodegenerative ...

  5. Machado–Joseph disease - Wikipedia

    en.wikipedia.org/wiki/Machado–Joseph_disease

    Machado–Joseph disease (MJD), also known as Machado–Joseph Azorean disease, Machado's disease, Joseph's disease or spinocerebellar ataxia type 3 (SCA3), is a rare autosomal dominantly inherited neurodegenerative disease that causes progressive cerebellar ataxia, [1] [2] which results in a lack of muscle control and coordination of the upper and lower extremities. [3]

  6. Terminal illness - Wikipedia

    en.wikipedia.org/wiki/Terminal_illness

    Terminal illness or end-stage disease is a disease that cannot be cured or adequately treated and is expected to result in the death of the patient. This term is more commonly used for progressive diseases such as cancer, dementia or advanced heart disease than for injury. In popular use, it indicates a disease that will progress until death ...

  7. Frontotemporal dementia - Wikipedia

    en.wikipedia.org/wiki/Frontotemporal_dementia

    Signs and symptoms. Frontotemporal dementia is an early onset disorder that mostly occurs between the ages of 45 and 65, [13] but can begin earlier, and in 20–25% of cases onset is later. [11][14] Men and women appear to be equally affected. [15] It is the most common early presenting dementia. [16]

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