Heterozygous deletion of the VEGFC gene in 4q34.3 is associated with Milroy‐like lymphedema: First prenatal case report

Deleterious variants in the vascular endothelial growth factor C (VEGFC) gene have been recently associated with Milroy‐like primary lymphedema, an autosomal dominant disorder, characterized mainly by swelling of the lower limbs due to functional impairment of the lymphatic vessels. To date, only 26...

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