The Lysosomal Storage Diseases: A Promising Axis for COVID-19 Future Therapies |Biomedgrid
Journal: American Journal of Biomedical Science & Research (Vol.10, No. 6)Publication Date: 2020-11-06
Authors : Naima Fdil; Miloud hammoud; Es-said Sabir; Karima Lafhal; Abdellatif Laamani; Sara Alibou; Wadii Ouahmane; Wafaa Fadili; Inass Laouad;
Page : 570-571
Keywords : COVID-19; Lysosomal storage disorders; Fabry disease; Glycosphingolipid; Hyperhidrosis;
Abstract
Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is the causative agent of the current COVID-19 pandemic; it has been officially named) by the WHO in March 2020 [1]. The current coronavirus pandemic is characterized by high contagion and infection rates and higher mortality among patients with some underlying medical conditions, including those with diabetes, high blood pressure, autoimmune diseases… Caring for high-risk populations is an essential part of managing any communicable disease threat. Patients with inherited metabolic diseases (IMD) are known to be disproportionately affected by respiratory diseases and recurrent infections often resulting in increased morbidity and mortality. IMD, like lysosomal storage diseases (LSD), were included in the group of conditions considered to have an extremely high risk of severe COVID-19 illness [2]. Respiratory symptoms are frequent in patients with LSD with pathomechanisms such as infiltration of pulmonary structures by abnormal cells in Niemann-Pick (NPD) and Gaucher diseases (GD), airway soft tissue infiltration, accompanied by limited chest mobility in mucchopolysaccharidoses diseases (MPSs), dyspnea and wheezing, with a compromised respiratory function by cardiac involvement in Fabry disease (FD) [3].
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