Progeria is a condition that resembles premature aging which usually refers specifically to Hutchinson-Gilford Progeria syndrome.
Hutchinson-Gilford Progeria syndrome is an extremely rare condition where symptoms resembling some aspects of aging are manifested at an early age, and few affected children live past age 13.
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Tags: Abnormal Growth, Aging Diseases Display Different Aspects, Cardiovascular Problems, Cell Nucleus, Childhood Disorder, Cockayne, Defective Dna Repair, Distinctive Appearance, Ftt, Genetic Condition, Genetic Test, Gilford Progeria Syndrome, Hgps, Hutchinson Gilford Progeria, Hutchinson Gilford Progeria Syndrome, Localized Scleroderma, Rare Condition, Skin Changes, Uniform Shape, Wrinkled Skin 
Comments OffAn DNA repair-deficiency disorder is a medical condition due to reduced functionality of DNA repair.
DNA repair defects are seen in nearly all of the diseases described as accelerated aging disease, in which various tissues, organs or systems of the human body age prematurely.
Posted in Diseases Tags: Aging Disease, Aging Diseases Display Different Aspects, Base Excision Repair, Biomarkers, Colorectal, Defective Mismatch Repair, Deficiency Diseases, Dna Repair Defects, Dna Repair Deficiency, Hereditary Nonpolyposis Colorectal Cancer, High Blood Pressure, Hnpcc, Hutchinson Gilford Progeria Syndrome, Medical Condition, Msh2 Gene, Progeria, Repair Dna, Symptoms Of Cancer, Systems Of The Human Body, Werner Syndrome Comments Off
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