Hutchinson-Gilford Progeria Syndrome and its Relevance to Cardiovascular Diseases and Normal Aging

Hutchinson-Gilford Progeria Syndrome and its Relevance to Cardiovascular Diseases and Normal Aging

Hutchinson-Gilford progeria syndrome（HGPS,OMIM176670）is an extremely rare,sporadic genetic syndrome with a reported prevalence of one in4-8million children worldwide.At April2012,the total number of known living children with HGPS was89worldwide,according to data from the Progeria Research Foundatio...

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Veröffentlicht in:Biomedical and environmental sciences 2013-05, Vol.26 (5), p.382-389
Hauptverfasser: QI, Ying Chun, XIE, Xiao Hua
Format: Artikel
Sprache:eng
Schlagworte:
Aging - physiology
Cardiovascular Diseases - complications
Humans
Phenotype
Progeria - complications
临床
医学理论
环境科学
生物医学
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Zusammenfassung:Hutchinson-Gilford progeria syndrome（HGPS,OMIM176670）is an extremely rare,sporadic genetic syndrome with a reported prevalence of one in4-8million children worldwide.At April2012,the total number of known living children with HGPS was89worldwide,according to data from the Progeria Research Foundation.
ISSN:0895-3988
2214-0190
DOI:10.3967/0895-3988.2013.05.007