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...

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Detalles Bibliográficos
Autores principales: Patil, Nikhil S., Iqbal, Munir M., Bursztyn, Lulu L. C. D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Case Report
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

Internet

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

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