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Progressive myoclonic epilepsy and horizontal gaze palsy: a rare aetiology
Gaucher’s disease is a rare autosomal recessive, potentially fatal disorder but most common type among lysosomal storage disorders. The disease’s incidence is around 1/40 000 to 1/60 000 births in the general population. A 32-year-old man, born out of non-consanguineous union, presented with general...
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| Publicado no: | BMJ Case Rep |
|---|---|
| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BMJ Publishing Group
2017
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5728210/ https://ncbi.nlm.nih.gov/pubmed/29237663 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/bcr-2017-222304 |
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