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Bart's Hemoglobinopathy

Known as: Hemoglobin Bart's Hydrops, Hemoglobin Barts 
A severe and rare form of alpha thalassemia characterized by the absence of alpha globin chains. It results in hydrops fetalis, severe anemia… 
National Institutes of Health

Papers overview

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2010
2010
Hemoglobin Barts hydrops fetalis syndrome is the most severe and generally fatal clinical phenotype of α-thalassemia. We… 
2008
2008
Routine laboratories use a hemoglobin H (HbH) screen to detect alpha-thalassemia carriers of fatal hemoglobin Bart's hydrops… 
2003
2003
alpha-Thalassemia trait is the most common inherited abnormality worldwide. Diagnosis of alpha-thalassemia trait can be difficult… 
1998
1998
Patients with the nondeletion genotype of hemoglobinopathy H (HbH or beta4) disease have higher proportions of HbH and more… 
1992
1992
A study on the incidence and gravity of malaria among children suffering of sickle cell anemia was carried out in the pediatric… 
1991
1991
The aim of this study was to determine the crude prevalence of alpha-thalassemia traits in Taiwan. A total of 1435 healthy… 
1989
1989
Funipuncture offers direct access to the fetal circulation. The blood gas and acid-base status of the fetus can be studied, and… 
Review
1986
Review
1986
Alpha-thalassemia is the most common cause of hydrops fetalis among Southeast Asians. With the recent influx of Southeast Asian…