Translated title of the contribution: WHIM syndrome

Research output: Contribution to journalReview article

1 Citation (Scopus)


The WHIM syndrome is a rare, autosomal dominant primary immunodeficiency disorder characterized by warts, hypogammaglobulinemia, recurrent infections, and myelokathexis. The authors summarize current knowledge on molecular basis, diagnostic criteria, therapy, and clinical manifestations of WHIM syndrome. The authors propose that delayed diagnosis and treatment of children with WHIM may be due to incomplete presentation of the disease.

Translated title of the contributionWHIM syndrome
Original languageHungarian
Pages (from-to)1173-1179
Number of pages7
JournalOrvosi hetilap
Issue number25
Publication statusPublished - Jun 24 2007

ASJC Scopus subject areas

  • Medicine(all)

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