Progeria Syndrome

Progeria Syndrome

Huntington's disease

Huntington's disease

Color Blindness

Color Blindness

Friday, April 23, 2010

Progeria syndrome is an extremely rare genetic disorder of unknown origin that manifests as premature aging in children. Progeria affects many parts of the body including the skin, bones, and arteries.Most patients appear normal at birth. Signs and symptoms usually begin to develop within the first one to two years of life. Changes in skin and failure to gain weight are usually noticeable first.There is presently no treatment for progeria

3 comments:

  1. Growth failure during the first year of life
    Narrow, shrunken or wrinkled face
    Baldness
    Loss of eyebrows and eyelashes
    Short stature
    Large head for size of face (macrocephaly)
    Open soft spot (fontanelle)
    Small jaw (micrognathia)
    Dry, scaly, thin skin
    Limited range of motion
    Teeth - delayed or absent formation

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