A NOVEL FLT4 GENE MUTATION AND MR LYMPHANGIOGRAPHY IN A CHINESE FAMILY WITH MILROY DISEASE
Abstract
Milroy disease is a congenital onset lymphedema linked to FLT4 gene mutations in the tyrosine kinase domain. So far, a total of 59 different FLT4 variants have been identified. Here, we report a novel FLT4 gene mutation in a Chinese family with Milroy disease and present their clinical symptoms and MR lymphangiographic findings.
Keywords: Milroy disease, FLT4, VEGFR-3, primary lymphedema, novel gene mutation, MR lymphangiogram, phenotype
How to Cite:
Liu, N., Yu, Z., Luo, Y., Sun, D. & Yan, Z., (2015) “A NOVEL FLT4 GENE MUTATION AND MR LYMPHANGIOGRAPHY IN A CHINESE FAMILY WITH MILROY DISEASE”, Lymphology 48(2), 93-96.
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