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Association d'une drepanocytose heterozygote et d'un deficit en G6PD: a propos d'un cas
Tunisie Medicale [La]. 1995; 73 (10): 415-7
in French | IMEMR | ID: emr-39860
ABSTRACT
The sickle cell trait is usually asymptomatic the ocurence of or sharp hemolysis should incite us to look for enzyme defect particularly associated to G6PD deficiency. We report the case of a 7 years child presenting with hemolytic anemia. The Hemoglobin and enzymatic studies allowed the diagnosis. This association is discussed through the literature
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Index: IMEMR (Eastern Mediterranean) Main subject: Sickle Cell Trait / Hemolysis Language: French Journal: Tunisie Med. Year: 1995

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Index: IMEMR (Eastern Mediterranean) Main subject: Sickle Cell Trait / Hemolysis Language: French Journal: Tunisie Med. Year: 1995