Fabry disease and multiple sclerosis misdiagnosis: the role of family history and neurological signs

Fabry disease (FD) is an X-linked inherited lysosomal storage disorder caused by α galactosidase A (α-gal A) deficiency. Central nervous system involvement and chronic white matter lesions are observed in both FD and multiple sclerosis (MS), which can confound the differential diagnosis. We analyzed...

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Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Cyhoeddwyd yn:Oncotarget
Prif Awduron: Colomba, Paolo, Zizzo, Carmela, Alessandro, Riccardo, Cammarata, Giuseppe, Scalia, Simone, Giordano, Antonello, Pieroni, Maurizio, Sicurella, Luigi, Amico, Luisa, Burlina, Alessandro, Duro, Giovanni
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: Impact Journals LLC 2018
Pynciau:
Research Paper: Pathology
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC5814255/
https://ncbi.nlm.nih.gov/pubmed/29487688
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.18632/oncotarget.23970
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