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Please use this identifier to cite or link to this item: http://hdl.handle.net/10400.18/952

Título: No ocular involvement in familial amyloidotic polyneuropathy ATTR V30M domino liver recipients
Autor: Melo Beirão, J.
Matos, E.
Beirão, I.
Costa, P.
Torres, P.
Palavras-chave: Familial Amyloidotic Polyneuropathy
Transplantation
Liver
Domino
Doenças Genéticas
Issue Date: Jun-2012
Editora: Springer Verlag
Citação: Transpl Int. 2012 Jun;25(6):646-51. Epub 2012 Mar 22
Resumo: In many transplantation centers domino liver transplantation is an established procedure, increasing the number of available liver grafts. Increasingly, grafts from familial amyloidotic polyneuropathy (FAP) patients are used. Ocular involvement is a well known manifestation of FAP, and can be vision-threatening. The aim of this study was to evaluate the risk of development of familial amyloidotic polyneuropathy ocular manifestations in domino liver recipients. Forty-four cirrhotic patients submitted to liver transplantation were studied, with an average of 6 years of follow up after the procedure. Twenty two patients had received a liver from a FAP donor (Group 1) and 22 had received a liver from a non-FAP cadaveric donor (Group 2). Both groups were similar for mean age and gender. Routine ophthalmological examinations with particular attention to amyloid deposition in the anterior segment and vitreous, peripheral retina state, lacrimal functions tests (Schirmer and tear break-up time) and pupillometry (dynamic and static) were performed. No statistically significant differences were observed in all studied ophthalmic parameters between the two groups. No FAP related ophthalmic manifestations were detected after 6 years of domino liver transplantation, but further prospective regular ophthalmological examinations are necessary to detect the eventual development of late ocular manifestations.
Arbitragem científica: yes
URI: http://hdl.handle.net/10400.18/952
ISSN: 0934-0874
Versão do Editor: http://onlinelibrary.wiley.com/doi/10.1111/j.1432-2277.2012.01467.x/full
Appears in Collections:DGH - Artigos em revistas internacionais

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