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1. Splice‐site mutations in VEGFC cause loss of function and Nonne‐Milroy‐like primary lymphedema.

Author

Fastré, E., Lanteigne, L‐e., Helaers, R., Giacalone, G., Revencu, N., Dionyssiou, D., Demiri, E., Brouillard, P., and Vikkula, M.

Subjects
*LYMPHEDEMA, *MESSENGER RNA, *GENETIC mutation, *PHYSIOLOGICAL therapeutics
Abstract

The article presents a case study of a 22 years old male with the Primary Lymphedema (PLE) due to the mutation in the VEGFC leading to loss of the function. Topics include the application of physiotherapy as the treatment for the patient, changes in the lymphocytic mRNA, and risk factors associated with the mutation.

Published
2018
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