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Diamond Blackfan Anemia

Medically Reviewed by The Medindia Medical Review Team on Oct 12, 2020


What is Diamond Blackfan Anemia?

It occurs when the bone marrow does not make sufficient red blood cells necessary for carrying oxygen from the lungs to other parts of the body. This makes the patient severely anemic. This kind of anemia is not due to insufficiencies in iron, vitamin B12, folate or erythropoietin. DBA is a life-threatening condition leading to other potential abnormalities. DBA affects approximately 5 to 7 per million live born infants worldwide.

Inheritance of Diamond Blackfan Anemia

Nearly 45% of DBA patients inherit the mutation from either of the affected parent. Some DBA patients present new mutations in the gene in families with no history of DBA.


Causes of Diamond Blackfan Anemia

Most people with DBA have mutations in the ribosomal protein gene. There are 12 genetic mutations linked to DBA. In rare cases, a mutation in a gene called GATA-1 is responsible for DBA in boys. GATA-1 is responsible for the earliest steps in red blood cell production.

Symptoms of Diamond Blackfan Anemia

Sometimes DBA presents itself in older children and adults. Symptoms include:

Some of the physical characteristics of DBA include:

People with DBA also present with cardiac and kidney defects. Eye problems such as cataracts, glaucoma and strabismus are not uncommon. Genitourinary abnormalities often occur in males.

Diagnosis/Testing of Diamond Blackfan Anemia

Other genetic anemias like Thalassemia and Fanconi's anemia need to be ruled out. Since a total of 13 genes (including GATA-1) are linked to DBA, mutations in nearly 55% of DBA patients are detectable through genetic sequencing of 9 genes.

Laboratory findings include:

Tests used to diagnose DBF include:

Treatment for Diamond Blackfan Anemia

Treatment options for DBA include:


Individuals with DBA are usually evaluated by haematologists, clinical geneticists, cardiologists, nephrologist and urologist (as required) and medical genetics counsellors. A multidisciplinary approach is critical to manage DBA and keep secondary complications in check.

Prevention of Secondary Complications

Individuals need to be assessed for iron overload in order to begin iron chelation therapy.

Measurements for iron overload include:


Iron chelation therapy to remove iron from the body needs to begin after 10-12 blood transfusions. The available options include:

Regular screening for related cancers is recommended for individuals with DBA.

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