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  • Title: [Hemoglobin Woodville associated with double point mutation in the gene of glucose-6-phosphate dehydrogenase].
    Author: Mansini AP, Fernández DA, Aguirre FM, Pepe C, Milanesio B, Chaves A, Eandi Eberle S, Feliú Torres A.
    Journal: Medicina (B Aires); 2015; 75(6):404-6. PubMed ID: 26707665.
    Abstract:
    The co-inheritance of erythrocyte defects, hemoglobinopathies, enzymopathies, and membranopathies is not an unusual event. For the diagnosis, a laboratory strategy, including screening and confirmatory tests, additional to molecular characterization, was designed. As the result of this approach, a 24-year-old man carrying a hemoglobinopathy (Hemoglobin Woodville) and an enzymopathy (glucose-6-phosphate dehydrogenase deficiency) was identified. In the heterozygous state hemoglobin Woodville, is asymptomatic, and homozygous or double heterozygous individuals have not been reported thus far. On the other hand, previously described double point mutation in the gene for glucose-6-phosphate dehydrogenase c. [202G>A; 376A>G], p. [Val 68Met; Asn126Asp], causes hemolysis of varying severity after food or drug intake or infections. This case highlights the importance of the methodology carried out for the diagnosis, treatment, and proper genetic counseling.
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