Immunohistochemical Evaluation of Histological Change in a Chinese Milroy Disease Family With Venous and Skin Abnormities
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DOI: 10.3389/fgene.2019.00206
Abstract: 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… read more here.
Keywords: milroy; milroy disease; family; evaluation ... See more keywords