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December 1974

Ocular Manifestations of Conradi Disease

Author Affiliations

From the Department of Ophthalmology of the University of Arkansas Medical Center, the Veterans Administration Hospital, and the Arkansas Children's Hospital, Little Rock, Ark.

Arch Ophthalmol. 1974;92(6):524-526. doi:10.1001/archopht.1974.01010010538016

Ocular findings in a case of Conradi disease (chondrodystrophia calcificans congenita) consisted of hypertelorism, epicanthus, mongoloid (upward) obliquity of lids, mild microphthalmia, iris synechiae, spherophakia, dense cataracts, and mild optic atrophy. The appearance of stippled epiphyses on x-ray film is diagnostic for Conradi disease.