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Alport syndrome with bilateral simultaneous anterior and posterior lenticonus with severe temporal macular thinning
Alport syndrome (AS) is a hereditary disease with various modes of inheritance, X-linked being the the most common. Anterior lenticonus is the characteristic abnormality along with perimacular and peripheral fleck retinopathy. Our two cases of AS had simultaneous anterior and posterior lenticonus wi...
Tallennettuna:
| Julkaisussa: | BMJ Case Rep |
|---|---|
| Päätekijät: | , , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
BMJ Publishing Group
2019
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6700549/ https://ncbi.nlm.nih.gov/pubmed/31420426 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/bcr-2019-229554 |
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