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  2. Ashley Treatment - Wikipedia

    en.wikipedia.org/wiki/Ashley_Treatment

    Ashley was born with a severe brain impairment of genetic cause, [2] termed a "static encephalopathy" because it does not improve. Although she sleeps and awakens, and breathes on her own, she is unable to raise her head, sit up, hold an object, walk, or talk, and must be tube-fed.

  3. Four Celebrities Who Suffered From Encephalopathy and Kept ...

    www.aol.com/news/four-celebrities-suffered...

    In 2005, Michael Crawford found out that he had ME (myalgic encephalopathy). ME affects many body systems, including the brain, making it harder for people with ME to do everyday activities. In ...

  4. Leukodystrophy - Wikipedia

    en.wikipedia.org/wiki/Leukodystrophy

    The X chromosome is a sex chromosome, and since women have two "chances" of acquiring a normal X chromosome (one maternal x, one paternal x), and males only one chance (one maternal x), this disease is more likely to be seen in males than in females. The mutation resulting in adult-onset leukodystrophy is mapped at 5q23.

  5. Encephalopathy - Wikipedia

    en.wikipedia.org/wiki/Encephalopathy

    Static encephalopathy: Unchanging, or permanent, brain damage, usually caused by prenatal exposure to ethanol. Uremic encephalopathy: Arising from high levels of toxins normally cleared by the kidneys—rare where dialysis is readily available. Wernicke's encephalopathy: Arising from thiamine (B 1) deficiency, usually in the setting of alcoholism.

  6. NYFW: Ashley Graham makes history at Michael Kors Fall ... - AOL

    www.aol.com/article/lifestyle/2017/02/16/nyfw...

    Michael Kors enlisted some of Hollywood's most in-demand models to walk in his show Wednesday -- and he made history doing it. NYFW: Ashley Graham makes history at Michael Kors Fall/Winter 2017 ...

  7. Leigh syndrome - Wikipedia

    en.wikipedia.org/wiki/Leigh_syndrome

    Leigh syndrome was first described by Denis Leigh in 1951 [21] and distinguished from similar Wernicke's encephalopathy in 1954. [9] In 1968, the disease's link with mitochondrial activity was first ascertained, though the mutations in cytochrome c oxidase and other electron transport chain proteins were not discovered until 1977. [7]