Erythrocyte pyruvate kinase deficiency. A case of severe congenital hemolytic anemia.
Mo Med
; 86(2): 92-4, 1989 Feb.
Article
in En
| MEDLINE
| ID: mdl-2761512
Although it occurs rarely, erythrocyte pyruvate kinase deficiency is a cause of neonatal jaundice and anemia across many ethnic and geographic groups. In this report of a Missouri case, an infant with this condition was also found to have Pelger-Huet leukocyte anomaly.
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Database:
MEDLINE
Main subject:
Pelger-Huet Anomaly
/
Pyruvate Kinase
/
Pyruvate Metabolism, Inborn Errors
/
Erythrocytes
/
Anemia, Hemolytic, Congenital
Type of study:
Diagnostic_studies
Limits:
Female
/
Humans
/
Newborn
Language:
En
Journal:
Mo Med
Year:
1989
Type:
Article