Novel mutations in the TBX5 gene in patients with Holt-Oram Syndrome

Autor(es)

Porto, Marianna P. R. ; Vergani, Naja ; Carvalho, Antonio Carlos C. ^[1] ; Cernach, Mirlene C. S. P. ; Brunoni, Decio ; Perez, Ana Beatriz A. ^[2]

Afiliação do(s) autor(es)

^[1] Univ Fed Sao Paulo, Dept Med, BR-04020041 Sao Paulo - Brazil

^[2] Univ Fed Sao Paulo, Dept Morfol, Ctr Genet Med, BR-04020041 Sao Paulo - Brazil

• Tipo de documento: Artigo Científico
• Fonte: GENETICS AND MOLECULAR BIOLOGY; v. 33, n. 2, p. 232-236, 2010.
• Citações Web of Science: 10

Resumo

The Holt-Oram syndrome (HOS) is an autosomal dominant condition characterized by upper limb and cardiac malformations. Mutations in the TBX5 gene cause HOS and have also been associated with isolated heart and arm defects. Interactions between the TBX5, GATA4 and NKX2.5 proteins have been reported in humans. We screened the TBX5, GATA4, and NKX2.5 genes for mutations, by direct sequencing, in 32 unrelated patients presenting classical (8) or atypical HOS (1), isolated congenital heart defects (16) or isolated upper-limb malformations (7). Pathogenic mutations in the TBX5 gene were found in four HOS patients, including two new mutations (c.374delG; c.678G > T) in typical patients, and the hotspot mutation c.835C > T in two patients, one of them with an atypical HOS phenotype involving lower-limb malformations. Two new mutations in the GATA4 gene were found in association with isolated upper-limb malformations, but their clinical significance remains to be established. A previously described possibly pathogenic mutation in the NKX2.5 gene (c.73C > 7) was detected in a patient with isolated heart malformations and also in his clinically normal father. (AU)

• Processo FAPESP: 03/01623-0 - Estudo dos genes envolvidos nos defeitos de membros superiores e cardiopatias
• Beneficiário: Ana Beatriz Alvarez Perez
• Linha de fomento: Auxílio à Pesquisa - Regular