Also, multiple syringofibroadenomas on the palms and soles and multiple eyelid hidrocystomas are distinctive for Schöpf-Schulz-Passarge syndrome, the autosomal recessive disease caused by WNT10A (Wnt Family Member 10A) gene mutation [16,17]. The gene discussed is WNT10A; the disease is Schöpf-Schulz-Passarge syndrome.