Hutchinson-Gilford progeria syndrome accompanied by severe skeletal abnormalities in two Chinese siblings: two case reports

INTRODUCTION: Hutchinson-Gilford progeria syndrome is a rare pediatric genetic syndrome with an incidence of one per eight million live births. The disorder is characterized by premature aging, generally leading to death due to myocardial infarction or stroke at approximately 13.4 years of age. The...

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Detalles Bibliográficos
Autores principales: Xiong, Zhimin, Lu, Yanmei, Xue, Jinjie, Luo, Sanchuan, Xu, Xiaojuan, Zhang, Lusi, Peng, Hao, Li, Wei, Chen, Dengming, Hu, Zhengmao, Xia, Kun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3602076/
https://www.ncbi.nlm.nih.gov/pubmed/23497705
http://dx.doi.org/10.1186/1752-1947-7-63

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3602076/
https://www.ncbi.nlm.nih.gov/pubmed/23497705
http://dx.doi.org/10.1186/1752-1947-7-63

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