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Cardiac manifestations in patients with classical or cardiac subtype of Fabry disease

BACKGROUND: Fabry disease (FD) is an X-linked lysosomal storage disorder engendered by a deficiency of the enzyme α-galactosidase A, leading to systemic accumulation of glycolipids. Studies have reported that the cardiac subtype of FD has a later onset and minimal extracardiac involvement. However,...

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Publicat a:J Chin Med Assoc
Autors principals: Wang, Wei-Ting, Sung, Shih-Hsien, Liao, Jo-Nan, Hsu, Ting-Rong, Niu, Dau-Ming, Yu, Wen-Chung
Format: Artigo
Idioma:Inglês
Publicat: Lippincott Williams & Wilkins 2020
Matèries:
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC7478196/
https://ncbi.nlm.nih.gov/pubmed/32649415
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/JCMA.0000000000000379
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