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Fifteen-minute consultation: Recognising primary immune deficiencies in children

Journal article
Authors Per Wekell
Olof Hertting
Daniel Holmgren
Anders Fasth
Published in Archives of Disease in Childhood: Education and Practice Edition
Volume 104
Pages 235-243
ISSN 1743-0585
Publication year 2019
Published at Institute of Clinical Sciences, Department of Pediatrics
Pages 235-243
Language en
Links dx.doi.org/10.1136/archdischild-201...
Keywords chronic granulomatous disease, hemophagocytic lymphohistiocytosis, primary immune deficiencies, severe combined immunodeficiency, severe congenital neutropenia,
Subject categories Pediatrics

Abstract

© Author(s) (or their employer(s)) 2019. No commercial re-use. See rights and permissions. Published by BMJ. Children with primary immunodeficiency syndromes present with broad variation of clinical features and the consequences are often severe if not promptly recognised. Here, support is provided for the general paediatrician to recognise primary immunodeficiencies among the many children they meet in their clinical practice.

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Denna text är utskriven från följande webbsida:
http://www.gu.se/english/research/publication/?publicationId=278198
Utskriftsdatum: 2019-12-06