Hutchinson-Gilford Progeria Syndrome: A Rare Genetic Disorder

Hutchinson-Gilford progeria syndrome (HGPS) is a rare pediatric genetic syndrome with incidence of one per eight million live births. The disorder is characterised by premature aging, generally leading to death at approximately 13.4 years of age. This is a follow-up study of a 9-year-old male with c...

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Dettagli Bibliografici
Autori principali: Panigrahi, Rajat G., Panigrahi, Antarmayee, Vijayakumar, Poornima, Choudhury, Priyadarshini, Bhuyan, Sanat K., Bhuyan, Ruchi, Maragathavalli, G., Pati, Abhishek Ranjan
Natura: Artigo
Lingua:Inglês
Pubblicazione: Hindawi Publishing Corporation 2013
Soggetti:
Case Report
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC3830809/
https://ncbi.nlm.nih.gov/pubmed/24288630
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2013/631378
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