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Please use this identifier to cite or link to this item: http://hdl.handle.net/10198/486

Título: Molecular characterization of a portuguese patient with Shwachman-Diamond syndrome
Autor: Lima, Rosa
Costa, Elísio
Rocha, Cristina
Vieira, Emília
Santos, Rosário
Barbot, José
Rocha, Herculano
Palavras-chave: SBDS
Shwachman-Diamond syndrome
Issue Date: 2005
Editora: Lippincott, Williams & Wilkins
Citação: Lima, 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. 115-116
Resumo: Shwachman-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).
URI: http://hdl.handle.net/10198/486
ISSN: 0277-2116
Appears in Collections:DTDT - Artigos em Revistas Indexados ao ISI/Scopus

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