Leukocyte adhesion deficiency mimicking Hirschsprung disease
- PMID: 7472832
- DOI: 10.1016/s0022-3476(95)70169-9
Leukocyte adhesion deficiency mimicking Hirschsprung disease
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.
Comment in
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Molecular cause of Hirschsprung disease.J Pediatr. 1996 May;128(5 Pt 1):720. doi: 10.1016/s0022-3476(96)80151-x. J Pediatr. 1996. PMID: 8627454 No abstract available.
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