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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Bibliografische gegevens
Hoofdauteurs: Panigrahi, Rajat G., Panigrahi, Antarmayee, Vijayakumar, Poornima, Choudhury, Priyadarshini, Bhuyan, Sanat K., Bhuyan, Ruchi, Maragathavalli, G., Pati, Abhishek Ranjan
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: Hindawi Publishing Corporation 2013
Onderwerpen:
Case Report
Online toegang: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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