[Early detection of WHIM symdrome. A case report].

Rev Alerg Mex

Laboratorio de Inmunodeficiencias, Instituto Nacional de Pediatría, Ciudad de México.

Published: May 2023

Background: WHIM syndrome corresponds to an inborn error of innate and intrinsic immunity, characterized by: warts (Warts), Hypogammaglobulinemia, Infections and Myelocathexis, for its acronym in English.

Case Report: 4-year-old male, with severe neutropenia and B-cell lymphopenia from birth, without severe infections or warts; the panel genetic sequencing study of primary immunodeficiencies with the CXCR4 c.1000C>T (p.Arg334*) variant, which is associated with WHIM syndrome.

Conclusions: The diagnosis of severe neutropenia from birth should include the search for inborn errors of immunity, through genetic sequencing studies, especially in asymptomatic or oligosymptomatic patients.

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http://dx.doi.org/10.29262/ram.v70i1.1211DOI Listing

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