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Molecular characterization of a portuguese patient with Shwachman-Diamond syndrome

dc.contributor.authorLima, Rosa
dc.contributor.authorCosta, Elísio
dc.contributor.authorRocha, Cristina
dc.contributor.authorVieira, Emília
dc.contributor.authorSantos, Rosário
dc.contributor.authorBarbot, José
dc.contributor.authorRocha, Herculano
dc.date.accessioned2008-02-18T10:21:17Z
dc.date.available2008-02-18T10:21:17Z
dc.date.issued2005
dc.description.abstractShwachman-Diamond syndrome (SDS) a rare autosomal recessive disorder described first time 1964 (1), is characterized by the association of exocrine pancreatic and bone marrow dysfunction. Other systemic findings (skeletal, liver and psychomotor) or problems secondary to bone marrow dysfunction may also be detected (1–4). Intermittent or persistent neutropenia is the most common hematologic finding, but anemia and thrombocytopenia are present in approximately 40% of the patients (1–4). In 2002, fine mapping identified the locus for SDS in band 7q11. More recently Boocock et al. (5) identified 18 positional candidate genes in this locus and examined eight of them for occurrence SDS-associated changes. They found alterations only in a previously uncharacterised gene. This gene, designated SBDS (Shwachman- Bodian-Diamond syndrome), is composed of five exons spanning 7.9Kb. The authors also described a pseudogene (SBDSP) with 97% homology to SBDS (5).
dc.identifier.citationLima, Rosa; Costa, Elísio; Rocha, Cristina; Vieira, Emília; Santos, Rosário; Barbot, José; Rocha, Herculano (2005). Molecular characterization of a portuguese patient with shwachman-diamond syndrome. Journal of Pediatric Gastroenterology and Nutrition. ISSN 0277-2116. 41:1 p. 115-116en
dc.identifier.issn0277-2116
dc.identifier.urihttp://hdl.handle.net/10198/486
dc.language.isoengen
dc.publisherLippincott, Williams & Wilkinsen
dc.subjectSBDSen
dc.subjectShwachman-Diamond syndromeen
dc.titleMolecular characterization of a portuguese patient with Shwachman-Diamond syndromeen
dc.typejournal article
dspace.entity.typePublication
rcaap.rightsopenAccess
rcaap.typearticleen

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