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Diamond–Blackfan anemia

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Title: Diamond–Blackfan anemia  
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Subject: Fragile X-associated tremor/ataxia syndrome, Nutritional anemia, Delta-thalassemia, Hexokinase deficiency, Hereditary persistence of fetal hemoglobin
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Diamond–Blackfan anemia

Diamond–Blackfan anemia
Classification and external resources
ICD-10 D61.0
ICD-9-CM 284.01
OMIM 105650
DiseasesDB 29062
eMedicine article/205695-overview/
MeSH D029503

Diamond–Blackfan anemia (DBA), also known as Blackfan-Diamond anemia, inherited pure red cell aplasia[1] and as inherited erythroblastopenia,[2] is a congenital erythroid aplasia that usually presents in infancy.[3] DBA causes low red blood cell counts (anemia), without substantially affecting the other blood components (the platelets and the white blood cells), which are usually normal. This is in contrast to Shwachman–Bodian–Diamond syndrome, in which the bone marrow defect results primarily in neutropenia, and Fanconi anemia, where all cell lines are affected resulting in pancytopenia.

A variety of other congenital abnormalities may also occur in DBA.

Clinical features

Diamond–Blackfan anemia is characterized by normocytic(cite) or macrocytic(cite) anemia (low red blood cell counts) with decreased erythroid progenitors in the bone marrow. This usually develops during the neonatal period. About 47% of affected individuals also have a variety of congenital abnormalities, including craniofacial malformations, thumb or upper limb abnormalities, cardiac defects, urogenital malformations, and cleft palate. Low birth weight and generalized growth delay are sometimes observed. DBA patients have a modest risk of developing leukemia and other malignancies.


Typically, a diagnosis of DBA is made through a blood count and a bone marrow biopsy.

A diagnosis of DBA is made on the basis of anemia, low reticulocyte (immature red blood cells) counts, and diminished erythroid precursors in bone marrow. Features that support a diagnosis of DBA include the presence of congenital abnormalities, macrocytosis, elevated fetal hemoglobin, and elevated adenosine deaminase levels in red blood cells.[4]

Most patients are diagnosed in the first two years of life. However, some mildly affected individuals only receive attention after a more severely affected family member is identified.

About 20–25% of DBA patients may be identified with a genetic test for mutations in the RPS19 gene.


First noted by Joseph in 1936,[1]:485[5] the condition is however named for Diamond and Blackfan, who described congenital hypoplastic anemia in 1938.[6] Responsiveness to corticosteroids was reported in 1951.[1]:485 In 1961, Diamond and colleagues presented longitudinal data on 30 patients and noted an association with skeletal abnormalities.[7] In 1997, a region on chromosome 19 was determined to carry a gene mutated in some DBA.[8][9] In 1999, mutations in the ribosomal protein S19 gene (RPS19) were found to be associated with disease in 42 of 172 DBA patients.[10] In 2001, a second DBA gene was localized to a region of chromosome 8, and further genetic heterogeneity was inferred.[11] Additional genes were subsequently identified.[12]


Most pedigrees suggest an autosomal dominant mode of inheritance[1] with incomplete penetrance.[13] Approximately 10–25% of DBA occurs with a family history of disease.

With the exception of DBA rarely arising from mutation of transcription factor GATA1,(add citation) DBA arises from abnormal ribosomal protein genes.[1] The disease is characterized by genetic heterogeneity, affecting different ribosomal gene loci:[12]

DBA types
name chromosome genotype[12] phenotype protein disruption(cite)(cite)
DBA1[12] 19q13.2 603474 105650 RPS19 30S to 18S[14]:291(cite)
DBA2 8p23-p22 unknown 606129
DBA3 10q22-q23 602412 610629 RPS24[15] 30S to 18S[14]:291(cite)
DBA4 15q 180472 612527 RPS17[16] 30S to 18S[14]:291
DBA5 3q29-qter 180468 612528 RPL35A[17] 32S to 5.8S/28S[14]:291(cite)
DBA6 1p22.1 603634 612561 RPL5[18] 32S to 5.8S/28S[14]:291
DBA7 1p36.1-p35 604175 612562 RPL11[18] 32S to 5.8S/28S[14]:291
DBA8 2p25 603658 612563 RPS7[18] 30S to 18S[14]:291
DBA9 6p 603632 613308 RPS10[12] 30S to 18S[19]
DBA10 12q 603701 613309 RPS26 30S to 18S[20]
DBA11 17p13 603704 614900 RPS26 30S to 18S[20]
DBA12 3p24 604174 615550 RPL15 45S to 32S[21]
DBA13 14q 603633 615909 RPS29
"other" TSR2,[22]RPS28,[22] GATA1

In 1997, a patient was identified who carried a rare balanced chromosomal translocation involving chromosome 19 and the X chromosome. This suggested that the affected gene might lie in one of the two regions that were disrupted by this cytogenetic anomaly. Linkage analysis in affected families also implicated this region in disease, and led to the cloning of the first DBA gene. About 20–25% of DBA cases are caused by mutations in the ribosome protein S19 (RPS19) gene on chromosome 19 at cytogenetic position 19q13.2. Some previously undiagnosed relatives of DBA patients were found to carry mutations, and also had increased adenosine deaminase levels in their red blood cells, but had no other overt signs of disease.

A subsequent study of families with no evidence of RPS19 mutations determined that 18 of 38 families showed evidence for involvement of an unknown gene on chromosome 8 at 8p23.3-8p22.[23] The precise genetic defect in these families has not yet been delineated.

Malformations are seen more frequently with DBA6 RPL5 and DBA7 RPL11 mutations.[13]

The genetic abnormalities underpinning the combination of DBA with Treacher Collins syndrome (TCS)/mandibulofacial dysostosis (MFD) phenotypes are heterogeneous, including RPS26 (the known DBA10 gene), TSR2 which encodes a direct binding partner of RPS26, and RPS28.[22]

DBA Mutation Database.

Molecular basis

The phenotype of DBA patients suggests a hematological stem cell defect specifically affecting the erythroid progenitor population. Loss of ribosomal function might be predicted to affect translation and protein biosynthesis broadly and impact many tissues. However, DBA is characterized by dominant inheritance, and arises from partial loss of ribosomal function, so it is possible that erythroid progenitors are more sensitive to this decreased function, while most other tissues are less affected.


adverse events from BMTs may exceed those from iron overloading.[25] An article published on Feb. 10, 2009 [1] reported that an eight-year-old boy with a DBA-like disease has been successfully treated by supplementing his diet with the amino acids leucine and isoleucine. A 2007 study[26] shows the efficacy of a similar treatment on a different patient. Larger studies are being conducted.

See also


  1. ^ a b c d e
  2. ^
  3. ^
  4. ^
  5. ^
  6. ^
  7. ^
  8. ^
  9. ^
  10. ^
  11. ^
  12. ^ a b c d e Online Mendelian Inheritance in Man. Diamond-Blackfan anemia. Johns Hopkins University. [2]
  13. ^ a b
  14. ^ a b c d e f g
  15. ^
  16. ^
  17. ^
  18. ^ a b c
  19. ^ Online 'Mendelian Inheritance in Man' (OMIM) 603632
  20. ^ a b Online 'Mendelian Inheritance in Man' (OMIM) 603701
  21. ^ Online 'Mendelian Inheritance in Man' (OMIM) 604174
  22. ^ a b c
  23. ^
  24. ^
  25. ^
  26. ^

External links

  • Diamond Blackfan Anemia Foundation (USA)
  • Daniella Maria Arturi Foundation Research For The Cure (USA)
  • GeneReviews/NCBI/NIH/UW entry on Diamond–Blackfan Anemia
  • OMIM entries on Diamond–Blackfan Anemia
  • Diamond–Blackfan Anemia research study of Inherited Bone Marrow Failure Syndromes (IBMFS)
  • UK Diamond Blackfan Anaemia Charity
  • Diamond Blackfan Anæmia International Support Group
  • Diamond Blackfan Anemia Registry of North America (DBAR)
  • Diamond–Blackfan anemia Genetics Home Reference
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