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
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what are the symptoms
ReplyDeleteGrowth failure during the first year of life
ReplyDeleteNarrow, 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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