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| Medical Condition: |
Hutchinson-Gilford Progeria Syndrome
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| Also Known As: |
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Progeria
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| Description: |
This is a rare and fatal genetic condition children begin to display symptoms at about a year and a half – they begin to age rapidly loosing body fat and hair, with aging skin and stiffness of the joints, the children’s life expectancy is up to 21.
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Please Note: The information provided here should not be used for diagnosis or treatment of any medical condition. A medical practitioner should always be consulted for diagnosis and treatment of all medical conditions.
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