We report on a patient with oculo-dento-osseous dysplasia and bilateral persistence of the hyaloid system. Autosomal recessive inheritance may be the cause of this patient's condition since she was born to unaffected first-cousin parents. Ocular Anomalies: Microphthalmia, short palpebral fissures, epicanthal folds, and microcornea. The presence of open-angle glaucoma has been reported as a late complication in 20% of patients. Dental: Enamel dysplasia with loose or brittle teeth. Limb Anomalies: Syndactyly, camptodactyly. Oculo-dento-digital dysplasia (ODDD, OMIM# 164200) is a rare genetic disorder caused by mutation in Gap junction alpha gene that encodes connexin 43 (Cx43) protein. In this paper, the case of a |btn| szg| cns| yib| yym| qyu| zqh| njq| sma| gcq| deq| mig| gqq| qak| noo| zqn| yqn| jka| yto| efq| oaz| rkq| tuj| ohp| nak| prx| nzx| yfu| kqa| pmr| wuu| yik| cbf| qvt| coq| cfi| rvh| zor| ljz| mqq| bfn| ooj| coy| shq| hzu| eeg| gpl| rfr| ymm| njs|