Sickle Cell Anemia, Thalassemia
Conditions
Keywords
Thalassemia, Sickle cell anemia, Carrier detection, Prenatal Diagnosis, Genetic counseling
Brief summary
Since 1987, a screening for β Thalassemia in pregnant women is carried on in northern Israel, and from 1999 all the samples were tested also for Hgb S, Hgb C, Hgb D, Hgb O Arab and others. In this study, the investigators intend to summarize the results of this preventive program aiming to detect couples at risk for having offspring with Thalassemia or SCA, the compliance regard to genetic counseling and prenatal diagnosis and the incidence of new affected babies born.
Interventions
Summary of data
Sponsors
Study design
Eligibility
Inclusion criteria
All pregnant women tested and their husband in those cases that the woman test revealed abnormal hemoglobin.
Exclusion criteria
No
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Number of carriers detected | End of study |
Secondary
| Measure | Time frame |
|---|---|
| Couples referred for prenatal diagnosis | End of study |
Countries
Israel