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| 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 |
© 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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