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  2. Amyloidosis - Wikipedia

    en.wikipedia.org/wiki/Amyloidosis

    Amyloidosis of the central nervous system can have more severe and systemic presentations that may include life-threatening arrhythmias, cardiac failure, malnutrition, infection, or death. [14] Neuropathic presentation can depend on the etiology of amyloidosis. [14]

  3. Pronghorn - Wikipedia

    en.wikipedia.org/wiki/Pronghorn

    Though not an antelope, it is known colloquially in North America as the American antelope, prong buck, pronghorn antelope and prairie antelope, [5] because it closely resembles the antelopes of the Old World and fills a similar ecological niche due to parallel evolution. [6] It is the only surviving member of the family Antilocapridae. [7]

  4. Wild-type transthyretin amyloid - Wikipedia

    en.wikipedia.org/wiki/Wild-Type_Transthyretin...

    Wild-type transthyretin amyloid (WTTA), also known as senile systemic amyloidosis (SSA), [1] is a disease that typically affects the heart and tendons of elderly people. It is caused by the accumulation of a wild-type (that is to say a normal) protein called transthyretin.

  5. Bluetongue disease - Wikipedia

    en.wikipedia.org/wiki/Bluetongue_disease

    Electron micrograph of Bluetongue virus, scale bar = 50 nm. Bluetongue (BT) disease is a noncontagious, arthropod-borne viral disease affecting ruminants, [1] primarily sheep and other domestic or wild ruminants, including cattle, yaks, [2] goats, buffalo, deer, dromedaries, and antelope. [3]

  6. Alpha-1 antitrypsin deficiency - Wikipedia

    en.wikipedia.org/wiki/Alpha-1_antitrypsin_deficiency

    A1AD may cause several manifestations associated with liver disease, which include impaired liver function and cirrhosis. In newborns, alpha-1 antitrypsin deficiency can result in early onset jaundice followed by prolonged jaundice. Between 3% and 5% of children with ZZ mutations develop life-threatening liver disease, including liver failure. [9]

  7. Milroy's disease - Wikipedia

    en.wikipedia.org/wiki/Milroy's_disease

    Milroy's disease is also known as primary or hereditary lymphedema type 1A or early onset lymphedema. It is a very rare disease with only about 200 cases reported in the medical literature. Milroy's disease is an autosomal dominant condition caused by a mutation in the FLT4 gene which encodes the vascular endothelial growth factor receptor 3 ...

  8. Bird flu was detected in a pig, and it could be a tipping ...

    www.aol.com/bird-flu-detected-pig-could...

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  9. Multiple epiphyseal dysplasia - Wikipedia

    en.wikipedia.org/wiki/Multiple_epiphyseal_dysplasia

    Multiple epiphyseal dysplasia (MED), also known as Fairbank's disease, is a rare genetic disorder (dominant form: 1 in 10,000 births) that affects the growing ends of bones. Long bones normally elongate by expansion of cartilage in the growth plate (epiphyseal plate) near their ends.