A Cardiac Variant of Fabry Disease Diagnosed with Chance Urinary Mulberry Cells

Fabry disease is an X-linked lysosomal storage disorder caused by a deficiency of α-galactosidase A and is classified into two types: classical and variant. The classical type exhibits classic manifestations, but the variant type does not and is therefore difficult to identify sometimes. A 73-year-o...

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Detalles Bibliográficos
Autores principales: Onishi, Rina, Kanaoka, Koshiro, Sugiura, Junichi, Tokunaga, Motoko, Takemoto, Yasuhiro, Onoue, Kenji, Yamamoto, Yuta, Horii, Manabu, Saito, Yoshihiko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Japanese Society of Internal Medicine 2018
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6306526/
https://www.ncbi.nlm.nih.gov/pubmed/29984754
http://dx.doi.org/10.2169/internalmedicine.1177-18

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6306526/
https://www.ncbi.nlm.nih.gov/pubmed/29984754
http://dx.doi.org/10.2169/internalmedicine.1177-18

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