1.
J Pediatr
; 127(5): 755-7, 1995 Nov.
Artigo
em Inglês
| MEDLINE
| ID: mdl-7472832
RESUMO
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.