Characterization of vertigo and hearing loss in patients with Fabry disease
Abstract Background Fabry Disease (FD) is an X-linked hereditary lysosomal storage disorder which leads to a multisystemic intralysosomal accumulation of globotriaosylceramid (Gb3). Besides prominent renal and cardiac organ involvement, patients commonly complain about vestibulocochlear symptoms lik...
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| Автори: | , , , , , , , , , |
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| Формат: | Artigo |
| Мова: | Inglês |
| Опубліковано: |
BMC
2018-08-01
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| Серія: | Orphanet Journal of Rare Diseases |
| Предмети: | |
| Онлайн доступ: | http://link.springer.com/article/10.1186/s13023-018-0882-7 |
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