A Milroy case with FLT4/VEGFR3 mutation and an unusual skin biopsy
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DOI: 10.1111/bjd.17120
Abstract: Milroy's disease (MD; MIM# 153100) is a rare autosomal, dominantly inherited condition associated with primary lymphoedema. FLT4 (also known as VEGFR-3), -the only known causative gene of MD is responsible for the majority of MD… read more here.
Keywords: milroy case; unusual skin; flt4 vegfr3; case flt4 ... See more keywords