What is Diamond Blackfan Anemia? How is it diagnosed?

*This information is compiled from various medical sources with special attention given to the DBA Foundation and the Diamond
Blackfan Anemia Registry of North America

Where does the name come from?

Diamond Blackfan Anemia's name originated from the founder of the Hematology/Oncology branch at Children's
Hospital in Boston Louis K. Diamond M.D. and Chief of the Pediatric Department Kenneth D. Blackfan.

DBA in general:

Diamond Blackfan Anemia (DBA) is a blood condition, present at birth, which is characterized by a failure of
the bone marrow to produce red blood cells, other blood cells such as white cells and platelets are usually not
affected. By itself, the term "anemia" means low red cell counts. Unlike other types of anemia, DBA is a bone
marrow failure syndrome. It has also been linked to a genetic mutation in some individuals. Severe anemia is
frequently found at birth and the majority of individuals are diagnosed before their first birthday.

What causes it?
DBA occurs when the bone marrow fails to make adequate numbers of red blood cells. Scientists  are currently
studying the genes involved in DBA to see why it occurs. RPS-19 has been linked in 25% of DBA cases but not
having this gene does not mean you do not have DBA. Forty percent of the patients with DBA have a mutation
in a gene or genes located in a wide region in the short arm of chromosome 8 (8p22.3-23) but a candidate
gene has not been identified yet. There has been no success in pinpointing the genetic defect in the DBA
patients who have neither RPS-19 mutation nor chromosome 8p22.3-23 mutation.

According to the DBA Registry of America:

DBA can be either congenital (such as DBA) or acquired (such as TEC, infection associated, malignancy associated, from drugs/toxins, etc.).


Diagnosis?
In addition to a complete history and physical examination, other diagnostic tests are used to aid in the
diagnosis of DBA. Initially, blood work is performed to evaluate the degree of anemia and examine other body
systems. One particular blood test called the red cell ADA (adenosine deaminase) is usually present at
elevated levels in patients with DBA. In addition to blood tests, samples of bone marrow (Bone Marrow
Aspirate and Biopsy) are taken to examine all of the blood cell lines (red cells, white cells, and platelets),
genetic make up of the bone marrow, and the physical architecture of the bone marrow. Bone marrow biopsies
can confirm that the erythroid ( red cell ) precursors are depleted, which can point to viral infection
( Parvovirus B19 ) or DBA.

DBA sufferers usually have a very high MCV (Mean Cell Volume) so tend to have larger red blood cells, and a
higher percentage of fetal hemoglobin (Hb F) than normal, all which can be tested through bloods and bone
marrow biopsies. Doctors may also check the reticulocyte count. High reticulocyte counts point to conditions
where blood is being created normally but is being destroyed. Low counts indicate a lack of red cell production.
In DBA, reticulocyte counts are very low, and can be zero.
According to the Diamond Blackfan Anemia Registry of North America:
The diagnostic criteria for DBA are: age less than 1 year, moderate to severe macrocytic anemia,
reticulocytopenia (low retic count), normal bone marrow cellularity with a paucity of erythroid precursors.


Major criteria that support a DBA diagnosis are: the RPS19 mutation or a positive family history. Minor
supportive criteria are: elevated erythrocyte adenosine deaminase (eADA) activity (normal ADA is 0.20-0.98, in
DBA you see 0.45-5.11), congenital anomalies, elevated fetal hemoglobin, no evidence of another type of bone
marrow failure. [My notes say that you should have all the diagnostic criteria and a couple of the supporting
criteria to have classical DBA.]

A comparison of DBA and TEC (transient erythroblastopenia of childhood): DBA is inherited, TEC is aquired.
50% of DBA patients show some physical anomaly [she's including short stature here], no TEC patients do.
There are also some CBC count differences, but the main ones would be that DBA his increased eADA
while TEC doesn't, DBA has increase mean corpuscle volume (MCV - the size of the red blood cell), and
generally TEC has no increase in fetal hemoglobin except during recovery.














What is a normal hemoglobin level?
On average, normal hemoglobin levels range from 12 to 18 g/dL (grams per deciliter) of blood for both sexes.
For men, a normal hemoglobin count is between 14 and 18 g/dL; for women, the normal range is between 12
and 16g/dL. For children 12 to 16 g/dl.

Anemia in general...

Anemia occurs when the number of red blood cells (or the hemoglobin in them) falls below these normal ranges
and the body's organs and tissues receive less oxygen than needed to function properly. Although "normal" is
something that varies from person to person, if your numbers are below the ranges, then you may be feeling
worse than you should.
Learn more about Anemia from the
ANEMIA INSTITUTE.

Synonyms

-Anemia, Congenital Pure Red Cell
-Aplasia, Congenital Pure Red Cell
-Chronic Congenital Aregenerative Anemia
-Constitutional Erythroid Hypoplasia
-DBA
-DBS
-Diamond-Blackfan Anemia
-Erythrogenesis Imperfecta
-Estren-Dameshek variant of Fanconi Anemia
-Hypoplastic Congenital Anemia       


This information obtained from Children's Hospital Boston at
www.childrenshospital.org,  WebMD
at
www.webmd.com , www.anemia.com , http://www.icomm.ca/geneinfo/anemdb.htm,  Journal of
Pediatric Hematology and
The Diamond Blackfan Anemia Registry of North America
You treat a disease, you win, you lose. You treat a
person I'll guarantee you'll win.
-Hunter Patch Adams-
From the DBA Foundation

To date there are no definite tests to diagnose DBA. However, the uniform diagnostic criteria for all
cases are: (1) normochromic-macrocytic anemia presenting in 90% of cases in the first 12 months of life;
(2)profound reticulocytopenia; (3) normocellular marrow with a selective, marked deficiency of red cell
precursors;(4) increased serum levels of erythropoietin; (5) normal or slightly decreased white cell counts;
and (6) normal
or increased platelet counts. Fetal hemoglobin is usually increased.