Oculodentodigital Dysplasia
Oculodentodigital dysplasia is a rare genetic disorder caused by mutation in gap junction alpha gene that encodes connexin 43 protein. It has been diagnosed in <300 people worldwide, and the incidence is 1 in 10 million populations. It is a multisystem disorder, affects many parts of the body, pa...
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| Main Author: | |
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| Format: | Article |
| Language: | English |
| Published: |
Wolters Kluwer Medknow Publications
2024-01-01
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| Series: | Delhi Journal of Ophthalmology |
| Subjects: | |
| Online Access: | https://journals.lww.com/10.4103/DLJO.DLJO_118_23 |
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