Novel ocular findings in oculodentodigital dysplasia (ODDD): a case report and literature review
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DOI: 10.1080/13816810.2019.1571616
Abstract: ABSTRACT Background: Oculodentodigitaldysplasia (ODDD; MIM no. 164200) is a rare hereditary disorder caused by mutations in the gene GJA1.Ocular disorders included microcornea, cornea opacity and glaucoma. However, few studies described fundus findings. Materials and methods:… read more here.
Keywords: novel ocular; oculodentodigital dysplasia; ocular findings; dysplasia ... See more keywords