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- Title
RARE VARIANTS IN LAMA5 GENE ASSOCIATED WITH FLT4 AND FOXC2 MUTATIONS IN PRIMARY LYMPHEDEMA MAY CONTRIBUTE TO SEVERITY.
- Authors
Liu, N.-f.; Yu, Z.-y.; Sun, D.; Lou, Y.
- Abstract
The article focuses on laminin subunit alpha-5 gene variants forkhead box protein C2 (FOXC2) and Fms-related tyrosine kinase 4 (FLT4) and their contribution to severity. Topics include FOXC2 and FLT4's role in causing lymphedema-distichiasis syndrome and Milroy disease (MD), expansion of phenotypes using indocyanine green fluorescence lymphography and magnetic resonance lymphangiography, and enhancement of lymphatics in MD patients through indocyanine green fluorescent lymphography imaging.
- Subjects
LAMININ genetics; FOXP2 gene; LYMPHEDEMA; LYMPHANGIOGRAPHY; MAGNETIC resonance imaging; PATIENTS
- Publication
Lymphology, 2016, Vol 49, Issue 4, p192
- ISSN
0024-7766
- Publication type
Article