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Böök syn·drome (buk), [MIM*112300] premolar aplasia, hyperhidrosis, and premature canities; autosomal dominant trait.Böök syndrome An extremely rare autosomal dominant OMIM 112300 condition characterised by premolar aplasia, palmo-plantar hyperhidrosis and premature grey hair, described in a single Swedish family in 1950.Böök, Jan A., Swedish geneticist, 1915–. Böök syndrome - premolar aplasia, hyperhidrosis, and premature graying of hair.Böök syn·drome (buk sindrōm) [MIM*112300] Premolar aplasia, hyperhidrosis, and premature canities. |