Hematologically important mutations: Shwachman-Diamond syndrome.

نویسندگان

  • Elísio Costa
  • Rosário Santos
چکیده

Shwachman-Diamond syndrome (SDS) is a rare autosomal recessive disorder characterized by exocrine pancreatic insufficiency, bone marrow dysfunction, and skeletal abnormalities. The Shwachman-Bodian-Diamond syndrome (SBDS) gene was identified as a causative gene for SDS in 2003, and genetic analyses of SDS have been performed. Over the last 4 years, a number of different mutations affecting the SBDS gene have been described. In this report, a summary of documented SDS associated mutations is provided.

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عنوان ژورنال:
  • Blood cells, molecules & diseases

دوره 40 2  شماره 

صفحات  -

تاریخ انتشار 2008