A COVID-19 family cluster with retinitis pigmentosa and hypogammaglobulinemia
- PMID: 35198051
- PMCID: PMC8809126
- DOI: 10.4103/atm.atm_520_21
A COVID-19 family cluster with retinitis pigmentosa and hypogammaglobulinemia
Abstract
Hypogammaglobulinemia is a heterogeneous group of innate and acquired antibody deficiency with variable disease severity, recurrent pneumonia, and bronchiectasis. The outcome of COVID in patients with hypogammaglobulinemia is variable depending on age, comorbidities, type of immunodeficiency, and use of immunoglobulins. We report the favorable outcome of two family members diagnosed with DNAJC17-related retinitis pigmentosa and hypogammaglobulinemia syndrome and infected with SARS-CoV-2 following contact with their mother who had COVID-19. We describe the different immune dysfunction in these patients and their impact on the course and management of SARS-CoV-2 infection.
Keywords: COVID-19; hypogammaglobulinemia; outcome; retinitis pigmentosa.
Copyright: © 2022 Annals of Thoracic Medicine.
Conflict of interest statement
There are no conflicts of interest.
Figures
References
-
- Starr JC, Brasher GW, Dominguez J, Rao A. Retinitis pigmentosa and hypogammaglobulinemia. South Med J. 2006;99:989–91. - PubMed
LinkOut - more resources
Full Text Sources