Repositório Científico do Instituto Nacional de Saúde >
Departamento de Genética Humana >
DGH - Posters/abstracts em congressos internacionais >

Please use this identifier to cite or link to this item: http://hdl.handle.net/10400.18/627

Title: Migration of an ancestral dysferlin splicing mutation from the Iberian peninsula to South America
Authors: Vernengo, Luis
Oliveira, Jorge
Krahn, Martin
Vieira, Emília
Santos, Rosário
Carraso, Luisa
Negrão, Luis
Panuncio, Ana
Leturcq, France
Labelle, Veronique
Bronze-da-Rocha, Elsa
Mesa, Rosario
Pizzarossa, Carlos
Lévy, Nicolas
Rodrigues, Maria-Mirta
Keywords: DYSF
Founder effect
Portugal
Uruguay
c.1180_1180+7delAGTGCGTG
Doenças Genéticas
Issue Date: 2011
Publisher: Elsevier
Citation: Abstracts/Neuromuscular Disorders 21. 2011:677
Abstract: Miyoshi myopathy, LGMD2B and DMAT are primary dysferlinopathies that belong to a group of muscular dystrophies inherited in an autosomal recessive mode. Additional presentations range from isolated hyperCKemia to severe functional disability. LGMD2B involves predominantly the proximal muscles of the lower limbs whereas in Miyoshi myopathy the muscles involved are those of the posterior muscle compartment of the calf. DMAT is characterized by anterior tibial muscle weakness which rapidly progresses to the lower and upper proximal muscles. Onset is usually in young adults, but congenital and late-onset forms have also been reported. We present the first Uruguayan patient to have been diagnosed with Miyoshi myopathy and four Portuguese patients that carry a novel mutation in exon12/intron12 boundary: c.1180_1180 + 7delAGTGCGTG (r.1054_1284del) in the DYSF gene. Evidence of a founder effect due to a common ancestral origin of this mutation was detected in heterozygosity in four patients and in homozygosity in one patient. The homozygous patient has no proven inbreeding so it can be inferred that the mutation is identical by descent. All patients shared a common haplotypes block identical in state between markers Cy172-H32 and D2S211. We believe that it derives from a common mutational event which is ancestral because of the recombination between the mutated gene and the telomeric flanking marker D2S2113. As this haplotype is not common among the Portuguese population, it is very unlikely that these mutated DYSF alleles represent recurrent events. This is the sixth founder effect of the DYSF gene to be found in the world so far.
URI: http://hdl.handle.net/10400.18/627
ISSN: 0960-8966
Appears in Collections:DGH - Posters/abstracts em congressos internacionais

Files in This Item:

File Description SizeFormat
Oliveira, 2011 - WMS DYSF.pdf2.52 MBAdobe PDFView/Open
Statistics
FacebookTwitterDeliciousLinkedInDiggGoogle BookmarksMySpaceOrkut
Formato BibTex mendeley Endnote Logotipo do DeGóis 

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.

 

  © 2010 www.insa.pt - Todos os direitos reservados | Feedback Ministério da Saúde

Estamos no RCAAP Governo Português separator Ministério da Educação e Ciência   Fundação para a Ciência e a Tecnologia

Financiado por:

POS_C UE