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Genetic susceptibility to severe COVID-19 by Claudio Cappadona; Valeria Rimoldi; Elvezia Maria Paraboschi; Rosanna Asselta is a Medicine article available to read on EtoBox.

Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is the etiologic agent of the coronavirus disease 2019 (COVID-19) pandemic. Clinical manifestations of the disease range from an asymptomatic condition to life-threatening events and death, with more severe courses being associated with age, male sex, and comorbidities. Besides these risk factors, intrinsic characteristics of the virus as well as genetic factors of the host are expected to account for COVID-19 clinical heterogeneity. Genetic studies have long been recognized as fundamental to identify biological mechanisms underlying congenital diseases, to pinpoint genes/proteins responsible for the susceptibility to different inherited conditions, to highlight targets of therapeutic relevance, to suggest drug repurposing, and even to clarify causal relationships that make modifiable some environmental risk factors. Though these studies usually take long time to be concluded and, above all, to translate their discoveries to patients' bedside, the scientific community moved really fast to deliver genetic signals underlying different COVID-19 phenotypes. In this Review, besides a concise description of COVID-19 symptomatol

It is typically read by researchers, students, and practitioners in Medicine.

Author
Claudio Cappadona; Valeria Rimoldi; Elvezia Maria Paraboschi; Rosanna Asselta
Publisher
Elsevier BV
Published
2023
Language
EN
Field
Medicine (Health Sciences)