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Recommendations for presymptomatic genetic testing and management of individuals at risk for hereditary transthyretin amyloidosis
PURPOSE OF REVIEW: These recommendations highlight recent experience in genetic counselling for the severe autosomal-dominant, late-onset transthyretin familial amyloid polyneuropathy (TTR-FAP) disease, and present a structured approach towards identification and monitoring of asymptomatic carriers...
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| Publié dans: | Curr Opin Neurol |
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| Auteurs principaux: | , , , , , , |
| Format: | Artigo |
| Langue: | Inglês |
| Publié: |
Lippincott Williams & Wilkins
2016
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| Sujets: | |
| Accès en ligne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4739313/ https://ncbi.nlm.nih.gov/pubmed/26734953 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/WCO.0000000000000290 |
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