Hutchinson-Gilford progeria syndrome complicated with stroke: A report of 2 cases and literature review

BACKGROUND: Hutchinson–Gilford Progeria Syndrome (HGPS) is a ultrarare, fatal autosomal dominant disorder. The pathogenesis of the disease is a mutation in LMNA, which leads to the accumulation of progerin in cells, impairing the normal physiological functions. Stroke and transient ischemic attack s...

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Detalles Bibliográficos
Autores principales: Wang, Jingjing, Yu, Qinmei, Ma, Xiaohui, Yuan, Zhefeng, Mao, Jianhua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Pediatrics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9745312/
https://www.ncbi.nlm.nih.gov/pubmed/36523395
http://dx.doi.org/10.3389/fped.2022.1056225

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9745312/
https://www.ncbi.nlm.nih.gov/pubmed/36523395
http://dx.doi.org/10.3389/fped.2022.1056225

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