Ophthalmological Manifestations of Alkaptonuria
Alkaptonuria is rare autosomal recessive multisystem disease, caused by mutations in the homogentisine oxidase gene, which leads to the deposition of metabolites of homogentisic acid in organs and tissues (ochronosis).The purpose: to study spectrum of ophthalmic manifestations of alkaptonuria in Rus...
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| Main Authors: | , |
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| Format: | Article |
| Language: | Russian |
| Published: |
Ophthalmology Publishing Group
2022-04-01
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| Series: | Oftalʹmologiâ |
| Subjects: | |
| Online Access: | https://www.ophthalmojournal.com/opht/article/view/1780 |
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