Leukocyte adhesion deficiency mimicking Hirschsprung disease.
case_report · Level V
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- Record sourced from PubMed, PMID 7472832.
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Abstract
An infant had clinical signs suggestive of Hirschsprung disease as the initial manifestation of leukocyte adhesion deficiency. Chromosome studies showed a deletion of the distal third of the long arm of one chromosome 21, and flow cytometric studies confirmed the defective expression of CD18.
Medical subject headings
- Hirschsprung Disease
- Leukocyte-Adhesion Deficiency Syndrome