Other Names for this Disease
- Congenital lipomatosis of pancreas
- Lipomatosis of pancreas, congenital
- Pancreatic insufficiency and bone marrow dysfunction
- Shwachman-Bodian syndrome
What symptoms may be associated with Shwachman-Diamond syndrome?
What causes Shwachman-Diamond syndrome?
How is Shwachman-Diamond syndrome inherited?
As a result of the bone marrow dysfunction, individuals with Shwachman-Diamond syndrome have a higher-than-average chance of developing myelodysplastic syndrome (MDS) and aplastic anemia, which are disorders that affect blood cell production, and a cancer of blood-forming tissue known as acute myeloid leukemia (AML).
Mutations in the SBDS gene have been identified in about 90 percent of people with the characteristic features of Shwachman-Diamond syndrome. This gene provides instructions for making a protein whose function is unknown, although it is active in cells throughout the body. Researchers suspect that the SBDS protein may play a role in processing RNA (a molecule that is a chemical cousin of DNA). This protein may also be involved in building ribosomes, which are cellular structures that process the cell's genetic instructions to create proteins. It is unclear how SBDS mutations lead to the major signs and symptoms of Shwachman-Diamond syndrome.
In cases where no SBDS mutation is found, the cause of this disorder is unknown.
The mode or type of inheritance of Shwachman-Diamond syndrome in individuals without an identified SBDS mutation is unknown.
- Shwachman-Diamond syndrome. Genetics Home Reference (GHR). 2007; http://ghr.nlm.nih.gov/condition=shwachmandiamondsyndrome.
- Rommens JM, Durie PR. Shwachman-Diamond Syndrome. GeneReviews. 2008; http://www.ncbi.nlm.nih.gov/books/NBK1756/. Accessed 8/2/2012.
- Black V. Shwachman Syndrome. National Organization of Rare Disorders (NORD). 2009; http://www.rarediseases.org/search/rdbdetail_abstract.html?disname=Shwachman%20Syndrome. Accessed 7/9/2009.