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WHIM Syndrome: from Pathogenesis Towards Personalized Medicine and Cure

WHIM Syndrome: from Pathogenesis Towards Personalized Medicine and Cure

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_6698215

WHIM Syndrome: from Pathogenesis Towards Personalized Medicine and Cure

About this item

Full title

WHIM Syndrome: from Pathogenesis Towards Personalized Medicine and Cure

Publisher

New York: Springer US

Journal title

Journal of clinical immunology, 2019-08, Vol.39 (6), p.532-556

Language

English

Formats

Publication information

Publisher

New York: Springer US

More information

Scope and Contents

Contents

WHIM syndrome is a rare combined primary immunodeficiency disease named by acronym for the diagnostic tetrad of warts, hypogammaglobulinemia, infections, and myelokathexis. Myelokathexis is a unique form of non-cyclic severe congenital neutropenia caused by accumulation of mature and degenerating neutrophils in the bone marrow; monocytopenia and ly...

Alternative Titles

Full title

WHIM Syndrome: from Pathogenesis Towards Personalized Medicine and Cure

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_6698215

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_6698215

Other Identifiers

ISSN

0271-9142,1573-2592

E-ISSN

1573-2592

DOI

10.1007/s10875-019-00665-w

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