A novel mutation in the conserved sequence of vascular endothelial growth factor receptor 3 leads to primary lymphoedema

OBJECTIVE: To investigate whether lymphoedema in a Chinese family showed the hereditary and clinical characteristics of Milroy disease, an autosomal dominant form of congenital lymphoedema, typically characterized by chronic lower limb tissue swelling due to abnormal lymphatic vasculature developmen...

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Detalles Bibliográficos
Autores principales: Dai, Ting, Li, Bohan, He, Bo, Yan, Liwei, Gu, Liqiang, Liu, Xiaolin, Qi, Jian, Li, Ping, Zhou, Xiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2018
Materias:
Clinical Research Reports
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6134653/
https://www.ncbi.nlm.nih.gov/pubmed/29896974
http://dx.doi.org/10.1177/0300060518773264

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6134653/
https://www.ncbi.nlm.nih.gov/pubmed/29896974
http://dx.doi.org/10.1177/0300060518773264

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