alexa Progeria | Spain| PDF | PPT| Case Reports | Symptoms | Treatment

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  • Progeria

    HGPS is caused by a mutation in the gene called LMNA (pronounced “lamin-a”). The LMNA gene produces the lamin A protein which is the structural scaffolding that holds the nucleus of a cell together. The abnormal lamin A protein that causes Progeria is called progerin. Progerin makes the nucleus unstable. That cellular instability leads to the process of premature aging and disease in Progeria.
  • Progeria

    Meeting a medical practitioner

    Progeria is normally recognized in earliest stages or early youth when an infant shows the characteristic signs of premature aging. It's possible that your family specialist or your youngster's pediatrician will see these signs and side effects amid consistent checkups. In the event that you first notice changes in your youngster that could be signs and side effects of progeria, make a meeting with your child's doctor. After assessment, your child may be alluded to a medicinal hereditary qualities master.


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