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Preimplantation genetic diagnosis for α-thalassaemia in China

PURPOSE: To report the usage of PGD for α-thalassaemia with the - -(SEA) genotype. METHOD: A PGD protocol using fluorescent gap PCR was performed for 51 cycles on 43 couples with the - -(SEA) genotype. Allele drop-out and amplification failure rates were retrospectively analyzed. RESULTS: A total of...

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Detalles Bibliográficos
Autores principales: Xu, Yan-Wen, Zeng, Yan-Hong, Deng, Jie, Liu, Ying, Gao, Ling, Zhou, Can-Quan, Zhuang, Guang-Lun
Formato: Texto
Lenguaje:English
Publicado: Springer US 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2758951/
https://www.ncbi.nlm.nih.gov/pubmed/19813097
http://dx.doi.org/10.1007/s10815-009-9336-4
Descripción
Sumario:PURPOSE: To report the usage of PGD for α-thalassaemia with the - -(SEA) genotype. METHOD: A PGD protocol using fluorescent gap PCR was performed for 51 cycles on 43 couples with the - -(SEA) genotype. Allele drop-out and amplification failure rates were retrospectively analyzed. RESULTS: A total of 472 embryos were biopsied. Amplification was achieved in 390 blastomeres, accounting for an amplification rate of 82.6%. In total, 120 wild-type, 94 heterozygotes and 140 homozygous mutant embryos were diagnosed. The successful diagnosis rate was 75.0%. The ADO rate in 49 blastomeres from six donated embryos was 16.4%. One hundred and fifty four embryos were transferred, resulting in 25 clinical pregnancies with an implantation rate of 24.0%. CONCLUSIONS: Single-round fluorescent gap PCR is a feasible and effective strategy in the PGD for α-thalassaemia with the - -(SEA) genotype.