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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Bibliografski detalji
Glavni autori: Panigrahi, Rajat G., Panigrahi, Antarmayee, Vijayakumar, Poornima, Choudhury, Priyadarshini, Bhuyan, Sanat K., Bhuyan, Ruchi, Maragathavalli, G., Pati, Abhishek Ranjan
Format: Artigo
Jezik:Inglês
Izdano: Hindawi Publishing Corporation 2013
Teme:
Case Report
Online pristup: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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