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Conjunctival lymphangiectasia and retinal angiopathy in hereditary transthyretin amyloidosis
BACKGROUND: Hereditary transthyretin amyloidosis (ATTR amyloidosis) is a rare condition where a mutation in the transthyretin gene leads to systemic deposition of amyloid. The manifestations and prognosis of ATTR amyloidosis depends on the specific ATTR mutation, with over 100 mutations reported in...
| Autores principales: | , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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BioMed Central
2022
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8734248/ https://www.ncbi.nlm.nih.gov/pubmed/34991732 http://dx.doi.org/10.1186/s40942-021-00357-x |