Understanding how WHIM syndrome may present in clinical practice

Explore profiles based on real patient cases to learn more about the heterogeneous presentation and diagnostic challenges of WHIM syndrome.

  • 14-year-old caucasian WHIM syndrome patient

    Classic Case of WHIM Syndrome

    All four classic features of WHIM syndrome are present but not recognized concurrently

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    profiles_classic_case

  • 40-year-old caucasian WHIM syndrome patient

    Initial CVID Diagnosis

    Initial CVID diagnosis; delayed WHIM syndrome diagnosis informed by genetic testing

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    profiles_cvid_dx

  • 15-year-old caucasian WHIM syndrome patient

    WHIM Syndrome Without Warts

    WHIM syndrome diagnosis in the absence of warts

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    profiles_dx_without_warts

  • 14-year-old hispanic WHIM syndrome patient

    Missed Myelokathexis in Early Bone Marrow Biopsy

    Myelokathexis missed on bone marrow biopsy in early childhood

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    profiles_missed_myelokathexis

  • 25-year-old african-american WHIM syndrome patient

    Diagnosis by Family History and Genetic Testing

    WHIM syndrome diagnosis in newborn triggered genetic testing for parent

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    profiles_family_history_dx

  • 35-year-old asian WHIM syndrome patient

    HPV Skin Infections and Carcinoma In Situ

    HPV warts in childhood and cytopenia during EBV infection as a teen persisting in adulthood

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    profiles_skin_infections

CVID=common variable immunodeficiency. EBV=Epstein-Barr virus. HPV=human papillomavirus.

Note: Images are not of actual patients. Hypothetical patient profiles are based on real case studies.

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