| Literature DB >> 30733240 |
Per Wekell1,2, Olof Hertting3, Daniel Holmgren2,4, Anders Fasth2,5.
Abstract
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. © Author(s) (or their employer(s)) 2019. No commercial re-use. See rights and permissions. Published by BMJ.Entities:
Keywords: chronic granulomatous disease; hemophagocytic lymphohistiocytosis; primary immune deficiencies; severe combined immunodeficiency; severe congenital neutropenia,
Mesh：
Year: 2019 PMID： 30733240 DOI： 10.1136/archdischild-2018-315484
Source DB: PubMed Journal: Arch Dis Child Educ Pract Ed ISSN： 1743-0585 Impact factor: 1.309