[MIM*133200] a dermatosis characterized by hyperkeratotic plaques of bizarre, geographic configuration, associated with erythrodermic areas that may vary remarkably in size, shape, and position from day to day; hair, nares, and teeth are not affected; onset is usually in the first year of life; autosomal dominant or recessive inheritance, caused by mutation in the connexin gene encoding gap junction protein beta-3 (GJB3) on 1p.
