Erschienen in:
07.01.2021 | Original Article
TREC Screening for WHIM Syndrome
verfasst von:
Martin Oman Evans II, Maureen M. Petersen, Amer Khojah, Soma C. Jyonouchi, George S. Edwardson, Yasmin West Khan, James Albert Connelly, David Morris, Shamik Majumdar, David H. McDermott, Jolan E. Walter, Philip M. Murphy
Erschienen in:
Journal of Clinical Immunology
|
Ausgabe 3/2021
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Abstract
Purpose
T cell receptor excision circle (TREC) quantification is a recent addition to newborn screening (NBS) programs and is intended to identify infants with severe combined immunodeficiencies (SCID). However, other primary immunodeficiency diseases (PID) have also been identified as the result of TREC screening. We recently reported a newborn with a low TREC level on day 1 of life who was diagnosed with WHIM (warts, hypogammaglobulinemia, infections, myelokathexis) syndrome, a non-SCID primary immunodeficiency caused by mutations in the chemokine receptor CXCR4.
Methods
We have now retrospectively reviewed the birth and clinical histories of all known WHIM infants born after the implementation of NBS for SCID.
Results
We identified six infants with confirmed WHIM syndrome who also had TREC quantification on NBS. Three of the six WHIM infants had low TREC levels on NBS. All six patients were lymphopenic but only one infant had a T cell count below 1,500 cells/μL. The most common clinical manifestation was viral bronchiolitis requiring hospitalization. One infant died of complications related to Tetralogy of Fallot, a known WHIM phenotype.
Conclusion
The results suggest that WHIM syndrome should be considered in the differential diagnosis of newborns with low NBS TREC levels.
Trial Registration
Not applicable.