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Evans Syndrome in a Patient with Chromosome 22q11.2 Deletion Syndrome: A Case Report

1 Jan 2003

Abstract excerpt

One patient with a chromosome 22q11.2 deletion and Evans syndrome is reported in this paper. Microdeletions of 22q11.2 are the main etiology for DiGeorge syndrome, a disorder characterized by heart defects, immune deficiencies due to aplasia or hypoplasia of the thymus, and hypocalcemia. Evans syndrome refers to a hematological autoimmune disorder with autoimmune hemolytic anemia accompanied by immune...

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PMID: 12554529
DOI: 10.1080/0880010390158685

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Evans Syndrome in a Patient with Chromosome 22q11.2 Deletion Syndrome: A Case ReportPMID 12554529Read ↗

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