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Multiple retinal astrocytic hamartomas in siblings with lebers congenital amaurosis: a case series and review of literature
BACKGROUND: Leber’s congenital amaurosis (LCA) is a known inherited retinal disease (IRD) associated with severe visual loss, nystagmus, amaurotic pupils, oculo-digital sign and markedly reduced or absent electroretinograms (ERG). Retinal astrocytic hamartomas (RAH) is a benign vascularized glial tu...
Tallennettuna:
| Julkaisussa: | BMC Ophthalmol |
|---|---|
| Päätekijät: | , , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
BioMed Central
2020
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7510068/ https://ncbi.nlm.nih.gov/pubmed/32967644 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12886-020-01646-z |
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