Anemia, Blackfan Diamond
Anemia, Blackfan Diamond
National Organization for Rare Disorders, Inc.
It is possible that the main title of the report Anemia, Blackfan Diamond is not the name you expected. Please check the synonyms listing to find the alternate name(s) and disorder subdivision(s) covered by this report.
- Anemia, Congenital Pure Red Cell
- Aplasia, Congenital Pure Red Cell
- Congenital Hypoplastic Anemia
- Aase Syndrome
- Diamond-Blackfan Anemia
- Erythrogenesis Imperfecta
- Inherited Erythroblastopenia
- Hypoplastic Congenital Anemia
- Aase-Smith II Syndrome
Related Disorders List
Information on the following diseases can be found in the Related Disorders section of this report:
- Aplastic Anemia
- Fanconi's Anemia
Blackfan-Diamond anemia (BDA) is a rare blood disorder that is caused by a failure of the bone marrow to generate enough red blood cells. It is characterized by deficiency of red blood cells at birth (congenital hypoplastic anemia) as well as slow growth, abnormal weakness and fatigue, paleness of the skin, characteristic facial abnormalities, protruding shoulder blades (scapulae), webbing or abnormal shortening of the neck due to fusion of certain bones in the spine (cervical vertebrae), hand deformities, congenital heart defects, and/or other abnormalities. The symptoms and physical findings associated with Blackfan-Diamond Anemia vary greatly from case to case.
Blackfan-Diamond anemia is characterized by moderate to severe deficiency of red blood cells. People with Blackfan-Diamond anemia have low red blood cell counts, but their platelet and white cell counts are normal.
Symptoms include abnormal weakness, paleness, and tiredness (lethargy), and they are often first noticed at approximately one month of age. Approximately one-third of those affected have physical anomalies, such as abnormal thumbs, characteristic facial features, or a short neck. Short stature is common.
Facial anomalies may include a snub nose, widely separated eyes, and/or a protruding upper lip. The affected individual's neck may be webbed or shortened and immobile due to fused vertebrae and shoulder blades may be prominent.
Approximately 30 percent of those affected are diagnosed in the first three months of life. Ninety percent are diagnosed within the first year.
A substantial risk exists for the development of myelodysplastic syndrome or acute myeloid leukemia, as well as selected solid tumors such as osteosarcomas. In rare cases, due to severe anemia, congestive heart failure may occur.
The exact cause of Blackfan-Diamond anemia is not known at this time. There are at least three genes associated with this disorder, but only one has been fully identified at this time.
The gene that has been identified is located on chromosome 19 (19q13.2) and is known as RPS19 (ribosomal protein S19). The disease caused by change (mutation) of this change is inherited in an autosomal dominant pattern. There is some evidence that the disorder may be autoimmune in origin as well.
Chromosomes, which are present in the nucleus of human cells, carry the genetic information for each individual. Human body cells normally have 46 chromosomes. Pairs of human chromosomes are numbered from 1 through 22 and the sex chromosomes are designated X and Y. Males have one X and one Y chromosome and females have two X chromosomes. Each chromosome has a short arm designated "p" and a long arm designated "q". Chromosomes are further sub-divided into many bands that are numbered. For example, "chromosome 19q13.2" refers to band 13.2 on the long arm of chromosome 19. The numbered bands specify the location of the thousands of genes that are present on each chromosome.
Genetic diseases are determined by the combination of genes for a particular trait that are on the chromosomes received from the father and the mother.
Dominant genetic disorders occur when only a single copy of an abnormal gene is necessary for the appearance of the disease. The abnormal gene can be inherited from either parent, or can be the result of a new mutation (gene change) in the affected individual. The risk of passing the abnormal gene from affected parent to offspring is 50% for each pregnancy regardless of the sex of the resulting child.
All individuals carry a few abnormal genes. Parents who are close relatives (consanguineous) have a higher chance than unrelated parents to both carry the same abnormal gene, which increases the risk to have children with a recessive genetic disorder.
Blackfan-Diamond anemia is a very rare disorder that affects males and females in equal numbers and is equally represented among all ethnic groups. The incidence of BDA is reported as 7 cases per million of population.
Symptoms of the following disorders can be similar to those of Blackfan- Diamond Anemia. Comparisons may be useful for a differential diagnosis:
Aplastic Anemia is characterized by bone marrow failure. A total suppression or aplasia of the bone marrow is typical of Aplastic Anemia. The disorder may occur for unknown reasons or as the result of a toxic reaction to radiation, certain drugs, or chemicals. In rare cases, a tumor in the thymus may cause this disorder. The bone marrow may be classified as hypoplastic or aplastic. Hypoplasia occurs when the marrow is defective or incompletely developed, while in aplasia the bone marrow ceases developing any new tissue.
Fanconi's Anemia is a rare form of familial aplastic anemia. It is characterized by bone abnormalities, microcephaly, hypogenitalism and brown pigmentation of the skin. Complications include infections such as pneumonia and meningitis, hemorrhages, and leukemia. Other malignancies may also occur.
For more information on these disorders, choose "Aplastic" and "Fanconi" as your search terms in the Rare Disease Database.)
Guidelines for the diagnosis of Blackfan-Diamond anemia have been published by a team of physicians at the Toronto Hospital for Sick Children.
Blackfan-Diamond anemia is usually treated with adrenal corticosteroid drugs beginning as early as possible. Red blood cell transfusions may be used in conjunction with steroid treatments. Multiple blood transfusions can be associated with heart and liver problems, and excessive accumulations of iron in body tissues. Multiple transfusions (every 4-8 weeks) are ordered when the anemia is particularly severe and when the response to treatment with steroids is lee than expected. Infections must be carefully guarded against since they can cause worsening of the blood condition.
The only cure for BDA is bone marrow transplantation. However, finding the matching healthy bone marrow from a willing donor is difficult.
Genetic counseling will be of benefit to patients and their families.
Information on current clinical trials is posted on the Internet at www.clinicaltrials.gov. All studies receiving U.S. government funding, and some supported by private industry, are posted on this government web site.
For information about clinical trials being conducted at the NIH Clinical Center in Bethesda, MD, contact the NIH Patient Recruitment Office:
Tollfree: (800) 411-1222
TTY: (866) 411-1010
For information about clinical trials sponsored by private sources, contact:
There are at least eight clinical trials underway (Summer 2006) that are designed to study various aspects of Blackfan-Diamond anemia. For information on the following, contact the NIH Patient Recruitment Office (see above) or visit the www.clinicaltrials.gov web site.
The National Heart Lung and Blood Institute (NHLBI) is sponsoring a study of the use of the drug Rituximab to treat individuals with moderate plastic anemia, pure red cell aplasia, or Diamond-Blackfan anemia. The clinical trials identifier is: NCT00229619.
The National Institute of Diabetes and Digestive and Kidney Diseases is sponsoring a study aimed at improving the results of bone marrow transplantation for patients with severe congenital anemias. The clinical trials identifier is: NCT00061568.
St. Jude Children's Research Hospital is sponsoring a study of partially matched stem cell transplantation for patients with anemias that are resistant to treatment. The clinical trials identifier is: NCT00244010.
The pharmaceutical company Novartis is sponsoring a trial involving the drug Deferasirox for individuals with congenital disorders of the red blood cells. The clinical trials identifier is: NCT00235391.
The National Cancer Institute (NCI) is sponsoring a genetic study of cancer risk and gene identification in patients with inherited bone marrow disorders and their families. The clinical trial identifier is: NCT00056121.
Dr. Paul J. Orchard of the University of Minnesota is the lead researcher in a study of stem cell transplantation for bone marrow failures. The clinical trial identifier is: NCT00176878.
Alper BP. Diamond-Blackfan Anemia. In: NORD Guide to Rare Disorders. Lippincott Williams & Wilkins. Philadelphia, PA. 2003:365.
Kasper, DL, Fauci AS, Longo DL, et al., eds. Harrison's Principles of Internal Medicine. 16th ed. McGraw-Hill Companies. New York, NY; 2005:622.
Lichtman MA, Beutler E, Kipps TJ, Selisohn U, et al., eds. Williams Hematology. 7th ed. McGraw-Hill Companies. New York, NY; 2006:437-39.
Lipton JM. Diamond blackfan anemia: New paradigms for a "not so pure" inherited red cell aplasia. Semin Hematol. 2006;43:167-77.
Lieberman L. Dror Y. Advances in the understanding the genetic basis for bone-marrow failure. Curr Opin Pediatr. 2006;18:15-21.
Kuliev A, Rechitsky S, Tur-Kaspa I, Verlinsky Y. Preimplantation genetics: Improving access to stem cell therapy. Ann N Y Acad Sci. 2005;1054:223-27.
Gordon-Smith EC. Congenital bone marrow failure involving the red blood cells. Hematology. 2005;10 Suppl 1:312-15.
Federman N, Sakamoto KM. The genetic basis of bone marrow failure syndromes in children. Mol Genet Metab. 2005;86:100-09.
Bagby GC, Lipton JM, Sloand EM. Schiffer CA. Marrow failure. Hematology Am Soc Hematol Educ Program. 2004;:318-36
FROM THE INTERNET
McKusick VA, ed. Online Mendelian Inheritance In Man (OMIM). The Johns Hopkins University. Diamond-Blackfan Anemia; DBA. Entry Number; 105650: Last Edit Date; 3/22/2006.
McKusick VA, ed. Online Mendelian Inheritance In Man (OMIM). The Johns Hopkins University. Diamond-Blackfan Anemia 2; DBA2. Entry Number; 606129: Last Edit Date; 6/15/2005.
Diamond Blackfan Anemia. Children's Hospital Boston. nd. 2pp.
Diamond-Blackfan Anemia. SickKids. Page published on 2005-10-27. 1p.
Leblanc T. Blackfan-Diamond disease. Orphanet. June 2006. 2pp.
Diamond Blackfan Anemia Registry
Schneider Children's Hospital,
269-01 76th Avenue, Rm 255
New Hyde Park, NY 11040
71-73 Main Street
Chesterfield, S44 6UR
NIH/National Heart, Lung and Blood Institute
P.O. Box 30105
Bethesda, MD 20892-0105
Genetic and Rare Diseases (GARD) Information Center
PO Box 8126
Gaithersburg, MD 20898-8126
For a Complete Report
This is an abstract of a report from the National Organization for Rare Disorders, Inc.® (NORD). Cigna members can access the complete report by logging into myCigna.com. For non-Cigna members, a copy of the complete report can be obtained for a small fee by visiting the NORD website. The complete report contains additional information including symptoms, causes, affected population, related disorders, standard and investigational treatments (if available), and references from medical literature. For a full-text version of this topic, see http://www.rarediseases.org/search/rdblist.html.
The information provided in this report is not intended for diagnostic purposes. It is provided for informational purposes only. NORD recommends that affected individuals seek the advice or counsel of their own personal physicians.
It is possible that the title of this topic is not the name you selected. Please check the Synonyms listing to find the alternate name(s) and Disorder Subdivision(s) covered by this report
This disease entry is based upon medical information available through the date at the end of the topic. Since NORD's resources are limited, it is not possible to keep every entry in the Rare Disease Database completely current and accurate. Please check with the agencies listed in the Resources section for the most current information about this disorder.
For additional information and assistance about rare disorders, please contact the National Organization for Rare Disorders at P.O. Box 1968, Danbury, CT 06813-1968; phone (203) 744-0100; web site www.rarediseases.org or email firstname.lastname@example.org
Last Updated: 9/23/2007
Copyright 1987, 1990, 1991, 1994, 1996, 1997, 1998, 1999, 2006, 2007 National Organization for Rare Disorders, Inc.
Healthwise, Healthwise for every health decision, and the Healthwise logo are trademarks of Healthwise, Incorporated.