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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Detalles Bibliográficos
Autores principales: Panigrahi, Rajat G., Panigrahi, Antarmayee, Vijayakumar, Poornima, Choudhury, Priyadarshini, Bhuyan, Sanat K., Bhuyan, Ruchi, Maragathavalli, G., Pati, Abhishek Ranjan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2013
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3830809/
https://www.ncbi.nlm.nih.gov/pubmed/24288630
http://dx.doi.org/10.1155/2013/631378

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3830809/
https://www.ncbi.nlm.nih.gov/pubmed/24288630
http://dx.doi.org/10.1155/2013/631378

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