Leopard Syndrome is a extremely rare disease, autosomal dominant, characterized from a series of systemich anomalies (cutaneous, facial, genital etc), between which the cardiovascular anomalies they assume a relief rolesure, "Leopard" is an acronym that was introduced from Gorlin.
Leopard Syndrome: Clinical presentation, molecular analysis and genotypo-phenotypo correlation
Limongelli G.;Russo G.;
2006
Abstract
Leopard Syndrome is a extremely rare disease, autosomal dominant, characterized from a series of systemich anomalies (cutaneous, facial, genital etc), between which the cardiovascular anomalies they assume a relief rolesure, "Leopard" is an acronym that was introduced from Gorlin.File in questo prodotto:
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