Novel ARPC1B mutation identified in a patient with recurrent eosinophilia

Novel ARPC1B mutation identified in a patient with recurrent eosinophilia

Source: News-Medical

​Immunodeficiency disorders linked to cytoskeleton defects are rare and complex, often presenting with diverse clinical features.

Immunodeficiency disorders linked to cytoskeleton defects are rare and complex, often presenting with diverse clinical features. This case report highlights a patient with recurrent eosinophilia and a novel homozygous ARPC1B mutation, expanding our u… [1640 chars]

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