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Related Experiment Video

Updated: Jul 14, 2026

Whisker-signaled Eyeblink Classical Conditioning in Head-fixed Mice

Whisker-signaled Eyeblink Classical Conditioning in Head-fixed Mice

Published on: March 30, 2016

[WHIM syndrome].

Melinda Erdos¹, László Maródi

¹Debreceni Egyetem, Orvos- és Egészségtudományi Centrum Infektológiai és Gyermekimmunológiai Tanszék Debrecen. melinda.erdos@yahoo.com

|June 19, 2007

Summary

WHIM syndrome, a rare immunodeficiency, presents with warts, low antibodies, infections, and neutrophil issues. Delayed diagnosis in children may stem from incomplete disease presentation, impacting treatment.

Area of Science:

Immunology
Genetics
Pediatrics

Background:

WHIM syndrome is a rare, autosomal dominant primary immunodeficiency.
Characterized by warts, hypogammaglobulinemia, recurrent infections, and myelocathexis.
Understanding its molecular basis is crucial for diagnosis and treatment.

Observation:

Clinical manifestations can be variable.
Incomplete disease presentation may lead to delayed diagnosis in children.
Early identification is key for effective management.

Findings:

Current knowledge on molecular basis, diagnostics, therapy, and clinical features is summarized.
WHIM syndrome impacts multiple aspects of the immune system.
The disorder requires a comprehensive diagnostic and therapeutic approach.

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Last Updated: Jul 14, 2026

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Implications:

Improved diagnostic criteria can expedite identification of WHIM syndrome.
Timely treatment can mitigate the severity of recurrent infections.
Further research into incomplete presentations may improve pediatric care for WHIM syndrome.