Hutchinson–Gilford progeria syndrome with severe calcific aortic valve stenosis

Hutchinson–Gilford progeria syndrome (HGPS) is a rare premature aging syndrome that results from mutation in the Laminin A gene. This case report of a 12-year-old girl with HGPS is presented for the rarity of the syndrome and the classical clinical features that were observed in the patient. All pat...

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Detalles Bibliográficos
Autores principales: Hanumanthappa, Natesh B, Madhusudan, Ganigara, Mahimarangaiah, Jayaranganath, Manjunath, Cholenahally N
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications 2011
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3180988/
https://www.ncbi.nlm.nih.gov/pubmed/21976890
http://dx.doi.org/10.4103/0974-2069.84670

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3180988/
https://www.ncbi.nlm.nih.gov/pubmed/21976890
http://dx.doi.org/10.4103/0974-2069.84670

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