Immunohistochemical Evaluation of Histological Change in a Chinese Milroy Disease Family With Venous and Skin Abnormities

Background: Milroy disease (MD) is rare and autosomal dominant resulting from mutations of the vascular endothelial growth factor receptor-3 (VEGFR-3 or FLT4), which leads to dysgenesis of the lymphatic system. Methods: Here we report a Chinese MD family with 2 affected members of two generations. W...

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Detalles Bibliográficos
Autores principales: Zhang, Sijia, Chen, Xihui, Yuan, Lijuan, Wang, Shuyan, Moli, Dangzhi, Liu, Shujuan, Wu, Yuanming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6433936/
https://www.ncbi.nlm.nih.gov/pubmed/30941160
http://dx.doi.org/10.3389/fgene.2019.00206

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6433936/
https://www.ncbi.nlm.nih.gov/pubmed/30941160
http://dx.doi.org/10.3389/fgene.2019.00206

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