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An updated review on phenocopies of primary immunodeficiency diseases

Primary immunodeficiency diseases (PIDs) refer to a heterogenous group of disorders characterized clinically by increased susceptibility to infections, autoimmunity and increased risk of malignancies. These group of disorders present with clinical manifestations similar to PIDs with known genetic de...

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Detalles Bibliográficos
Autores principales: Singh, Ankita, Jindal, Ankur K., Joshi, Vibhu, Anjani, Gummadi, Rawat, Amit
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Chongqing Medical University 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7063430/
https://www.ncbi.nlm.nih.gov/pubmed/32181272
http://dx.doi.org/10.1016/j.gendis.2019.09.007
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author Singh, Ankita
Jindal, Ankur K.
Joshi, Vibhu
Anjani, Gummadi
Rawat, Amit
author_facet Singh, Ankita
Jindal, Ankur K.
Joshi, Vibhu
Anjani, Gummadi
Rawat, Amit
author_sort Singh, Ankita
collection PubMed
description Primary immunodeficiency diseases (PIDs) refer to a heterogenous group of disorders characterized clinically by increased susceptibility to infections, autoimmunity and increased risk of malignancies. These group of disorders present with clinical manifestations similar to PIDs with known genetic defects but have either no genetic defect or have a somatic mutation and thus have been labelled as “Phenocopies of PIDs”. These diseases have been further subdivided into those associated with somatic mutations and those associated with presence of auto-antibodies against various cytokines. In this review, we provide an update on clinical manifestations, diagnosis and management of these diseases.
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spelling pubmed-70634302020-03-16 An updated review on phenocopies of primary immunodeficiency diseases Singh, Ankita Jindal, Ankur K. Joshi, Vibhu Anjani, Gummadi Rawat, Amit Genes Dis Article Primary immunodeficiency diseases (PIDs) refer to a heterogenous group of disorders characterized clinically by increased susceptibility to infections, autoimmunity and increased risk of malignancies. These group of disorders present with clinical manifestations similar to PIDs with known genetic defects but have either no genetic defect or have a somatic mutation and thus have been labelled as “Phenocopies of PIDs”. These diseases have been further subdivided into those associated with somatic mutations and those associated with presence of auto-antibodies against various cytokines. In this review, we provide an update on clinical manifestations, diagnosis and management of these diseases. Chongqing Medical University 2019-09-24 /pmc/articles/PMC7063430/ /pubmed/32181272 http://dx.doi.org/10.1016/j.gendis.2019.09.007 Text en © 2019 Chongqing Medical University. Production and hosting by Elsevier B.V. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Singh, Ankita
Jindal, Ankur K.
Joshi, Vibhu
Anjani, Gummadi
Rawat, Amit
An updated review on phenocopies of primary immunodeficiency diseases
title An updated review on phenocopies of primary immunodeficiency diseases
title_full An updated review on phenocopies of primary immunodeficiency diseases
title_fullStr An updated review on phenocopies of primary immunodeficiency diseases
title_full_unstemmed An updated review on phenocopies of primary immunodeficiency diseases
title_short An updated review on phenocopies of primary immunodeficiency diseases
title_sort updated review on phenocopies of primary immunodeficiency diseases
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7063430/
https://www.ncbi.nlm.nih.gov/pubmed/32181272
http://dx.doi.org/10.1016/j.gendis.2019.09.007
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