Marfan syndrome with a complex chromosomal rearrangement including deletion of the FBN1 gene

• Autor(a) principal: Colovati, Mileny E. S. [UNIFESP]
• Data de Publicação: 2012
• Outros Autores: Silva, Luciana R. J. da [UNIFESP], Takeno, Sylvia S. [UNIFESP], Mancini, Tatiane I. [UNIFESP], Dutra, Ana R. N. [UNIFESP], Guilherme, Roberta S. [UNIFESP], Mello, Claudia B. de [UNIFESP], Melaragno, Maria I. [UNIFESP], Perez, Ana B. A. [UNIFESP]
• Tipo de documento: Artigo
• Idioma: eng
• Título da fonte: Repositório Institucional da UNIFESP
• Texto Completo: http://dx.doi.org/10.1186/1755-8166-5-5; http://repositorio.unifesp.br/handle/11600/34533
• topic: FBN1; Marfan syndrome; Complex Chromosomal Rearrangement

Background: the majority of Marfan syndrome (MFS) cases is caused by mutations in the fibrillin-1 gene (FBN1), mapped to chromosome 15q21.1. Only few reports on deletions including the whole FBN1 gene, detected by molecular cytogenetic techniques, were found in literature.Results: We report here on a female patient with clinical symptoms of the MFS spectrum plus craniostenosis, hypothyroidism and intellectual deficiency who presents a 1.9 Mb deletion, including the FBN1 gene and a complex rearrangement with eight breakpoints involving chromosomes 6, 12 and 15.Discussion: This is the first report of MFS with a complex chromosome rearrangement involving a deletion of FBN1 and contiguous genes. in addition to the typical clinical findings of the Marfan syndrome due to FBN1 gene haploinsufficiency, the patient presents features which may be due to the other gene deletions and possibly to the complex chromosome rearrangement.