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rdf:type |
|
|
lifeskim:mentions |
|
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pubmed:issue |
5
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pubmed:dateCreated |
1995-12-14
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|
pubmed:abstractText |
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.
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pubmed:commentsCorrections |
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
AIM
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|
pubmed:chemical |
|
|
pubmed:status |
MEDLINE
|
|
pubmed:month |
Nov
|
|
pubmed:issn |
0022-3476
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pubmed:author |
|
|
pubmed:issnType |
Print
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pubmed:volume |
127
|
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
755-7
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pubmed:dateRevised |
2005-11-16
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pubmed:meshHeading |
pubmed-meshheading:7472832-Antigens, CD11,
pubmed-meshheading:7472832-Antigens, CD18,
pubmed-meshheading:7472832-Chromosome Deletion,
pubmed-meshheading:7472832-Chromosomes, Human, Pair 21,
pubmed-meshheading:7472832-Diagnosis, Differential,
pubmed-meshheading:7472832-Fatal Outcome,
pubmed-meshheading:7472832-Hirschsprung Disease,
pubmed-meshheading:7472832-Humans,
pubmed-meshheading:7472832-Infant,
pubmed-meshheading:7472832-Leukocyte-Adhesion Deficiency Syndrome,
pubmed-meshheading:7472832-Male
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pubmed:year |
1995
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|
pubmed:articleTitle |
Leukocyte adhesion deficiency mimicking Hirschsprung disease.
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|
pubmed:affiliation |
Department of Pediatrics, University of Texas Medical School at Houston 77030, USA.
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pubmed:publicationType |
Journal Article,
Review,
Case Reports
|
