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Multimodal retinal imaging in a Chinese kindred with familial amyloid polyneuropathy secondary to transthyretin Ile107Met mutation

OBJECTIVE: To investigate the ocular phenotype and gene mutation of a Chinese pedigree with familial amyloid polyneuropathy (FAP) and vitreous amyloidosis. METHODS: A Chinese pedigree with familial amyloid polyneuropathy and vitreous amyloidosis was recruited. Combined phacoemulsification, vitrectom...

Ausführliche Beschreibung

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Bibliographische Detailangaben
Hauptverfasser: Lv, W, Chen, J, Chen, W, Hou, P, Pang, C P, Chen, H
Format: Artigo
Sprache:Inglês
Veröffentlicht: Nature Publishing Group 2014
Schlagworte:
Online Zugang:https://ncbi.nlm.nih.gov/pmc/articles/PMC3983639/
https://ncbi.nlm.nih.gov/pubmed/24480837
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/eye.2014.10
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