scholarly journals Persistent COVID-19 Infection in Wiskott-Aldrich Syndrome Cleared Following Therapeutic Vaccination: a Case Report

Author(s):  
Rachel E. Bradley ◽  
Mark J. Ponsford ◽  
Martin J. Scurr ◽  
Andrew Godkin ◽  
Stephen Jolles ◽  
...  
2016 ◽  
Vol 44 (5) ◽  
pp. 450-454 ◽  
Author(s):  
M. Eghbali ◽  
M. Sadeghi-Shabestari ◽  
F. Najmi Varzaneh ◽  
A. Zare Bidoki ◽  
N. Rezaei

2018 ◽  
Vol 19 (1) ◽  
Author(s):  
Hossein Esmaeilzadeh ◽  
Mohammad Reza Bordbar ◽  
Hassan Dastsooz ◽  
Mohammad Silawi ◽  
Mohammad Ali Farazi Fard ◽  
...  

2020 ◽  
Vol 40 (2) ◽  
pp. 206-210
Author(s):  
Anitha Santosh ◽  
Karun Banthiya ◽  
C.T. Deshmukh ◽  
Prasad Bhange ◽  
Shagun Shah ◽  
...  

2020 ◽  
Vol 11 ◽  
Author(s):  
Sabina Cenciarelli ◽  
Valeria Calbi ◽  
Federica Barzaghi ◽  
Maria Ester Bernardo ◽  
Chiara Oltolini ◽  
...  

In this work we present the case of SARS-CoV-2 infection in a 1.5-year-old boy affected by severe Wiskott-Aldrich Syndrome with previous history of autoinflammatory disease, occurring 5 months after treatment with gene therapy. Before SARS-CoV-2 infection, the patient had obtained engraftment of gene corrected cells, resulting in WASP expression restoration and early immune reconstitution. The patient produced specific immunoglobulins to SARS-CoV-2 at high titer with neutralizing capacity and experienced a mild course of infection, with limited inflammatory complications, despite pre-gene therapy clinical phenotype.


2020 ◽  
Vol 21 (1) ◽  
Author(s):  
Brigitte Glanzmann ◽  
Marlo Möller ◽  
Mardelle Schoeman ◽  
Michael Urban ◽  
Paul D. van Helden ◽  
...  

PM&R ◽  
2017 ◽  
Vol 9 ◽  
pp. S278-S278
Author(s):  
Ratnakar Veeramachaneni ◽  
Yuxi Chen ◽  
Ratnakar Veeramachaneni ◽  
Rahul Thomas ◽  
Anna Rozman

2011 ◽  
Vol 31 (2) ◽  
pp. 146-150 ◽  
Author(s):  
Mani Kant Kumar ◽  
Raghvendra Narayan

Wiskott-Aldrich syndrome is an X-linked recessive disorder characterized by thrombocytopenia, eczema and recurrent infections. We report a 15 month old boy who had presented with lower gastrointestinal bleed, recurrent infections and eczema. Blood picture revealed microthrombocytopenia, high IgA and IgE, and low IgM and Normal IgG levels. A diagnosis of Wiskott-Aldrich Syndrome was made, which was missed by many paediatrician even after prolonged hospital stay before admission in our Institute. The recent progress in understanding of the pathophysiology and treatment are discussed. Key words: Wiskott-Aldrich syndrome; Eczema; Microthrombocytopenia DOI: 10.3126/jnps.v31i2.4122 J Nep Paedtr Soc 2010;31(2):146-150


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