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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...
| Autores principales: | , , , , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
SAGE Publications
2018
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| Materias: | |
| 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 |