共查询到20条相似文献,搜索用时 100 毫秒
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Porto MP Vergani N Carvalho AC Cernach MC Brunoni D Perez AB 《Genetics and molecular biology》2010,33(2):232-236
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. 相似文献
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Holt-Oram syndrome (HOS) is a specific developmental defect involving upper limb malformations and cardiac defects. Mutations in the TBX5 gene, located on chromosome 12q24.1, were demonstrated as the underlying molecular defect in several families with this disorder. We report on two unrelated families with HOS. Affected members of both families have the same truncation mutation in exon 5 of the TBX5 gene (Y136X). This mutation has not been reported before in HOS. The spectrum of defects is similar in both families, displaying an ASD, hypoplastic deltoid muscles and hypoplastic or absent thumbs extending to radial defects in one case. So far, only a single genotype-phenotype analysis in HOS has been done which is not sufficient to explain the high inter- and intrafamilial variability of expression. Our observation further supports that the position of the mutation in the TBX5 gene is related to the phenotype expression of HOS. 相似文献
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Rallis C Bruneau BG Del Buono J Seidman CE Seidman JG Nissim S Tabin CJ Logan MP 《Development (Cambridge, England)》2003,130(12):2741-2751
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Chamber-specific cardiac expression of Tbx5 and heart defects in Holt-Oram syndrome. 总被引:10,自引:0,他引:10
B G Bruneau M Logan N Davis T Levi C J Tabin J G Seidman C E Seidman 《Developmental biology》1999,211(1):100-108
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J. A. Terrett R. Newbury-Ecob N. M. Smith Q. Y. Li C. Garrett P. Cox D. Bonnet S. Lyonnet A. Munnich A. J. Buckler J. D. Brook 《American journal of human genetics》1996,59(6):1337-1341
A gene for Holt-Oram syndrome (HOS) has been previously mapped to chromosome 12q2 and designated HOS1. We have identified a HOS patient with a de novo chromosomal rearrangement involving 12q. Detailed cytogenetic analysis of this case reveals three breaks on 12q, and two of these are within the HOS1 interval. By using a combination of chromosome painting and FISH with YACs and cosmids, it has been possible to map these breakpoints within the critical HOS1 interval and thus provide a focus for HOS gene-identification efforts. 相似文献