Ward Syndrome (Epitheliomatous Phakomatosis; Nevus-Jaw Cyst Syndrome) 1
General: Autosomal dominant.
Ocular: Hypertelorism; dystopia canthorum; nevi of eyelids; congenital cataracts; congenital corneal opacities; colobomata.
Clinical: Basal cell nevi with multiple basalomatous nodules on face, neck, and trunk; epithelioma adenoides cysticum.
Font RL, Ferry AP. The phakomatoses. Int Ophthalmol Clin 1972; 12:1.
Gorlin RJ, Goltz RW. Multiple nevoid basal-cell epithelioma, jaw cysts and bifid ribs. N Engl J Med 1960; 262:908.
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