
pmid: 2286030
Hemoglobinopathies are frequently occurring disorders for which prenatal diagnosis is possible. Couples in which one parent has microcytic hypochromic red blood cells; is of Southeast Asian, Mediterranean, Middle Eastern, Indian, or African origin; or had one previous child with a known hemoglobinopathy or a previous hydropic stillbirth should be investigated. The hemoglobinopathies have been the paradigm of prenatal diagnosis, and the lessons learned from their study are now being applied to a range of other genetic disorders for which the responsible genes have been identified.
Genetic Carrier Screening, Genetic Counseling, Anemia, Sickle Cell, Fetal Diseases, Pregnancy, Prenatal Diagnosis, Humans, Thalassemia, Female, Genetic Testing
Genetic Carrier Screening, Genetic Counseling, Anemia, Sickle Cell, Fetal Diseases, Pregnancy, Prenatal Diagnosis, Humans, Thalassemia, Female, Genetic Testing
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