THE LYMPHOEDEMA TREATMENT SINGAPORE DIARIES

Congenital lymphedema seems before age two a long time and is due to lymphatic aplasia or hypoplasia. Milroy condition is undoubtedly an autosomal dominant familial method of congenital lymphedema attributed to vascular endothelial development component receptor-3 (VEGFR-three) gene mutations and in some cases associated with cholestatic jaundice a