scholarly journals Preimplantation genetic diagnosis of X-linked diseases examined by indirect linkage analysis

2015 ◽  
Vol 116 (09) ◽  
pp. 542-546 ◽  
Author(s):  
I. Borgulova ◽  
M. Putzova ◽  
I. Soldatova ◽  
L. Krautova ◽  
L. Pecnova ◽  
...  
Keyword(s):  
Linkage Analysis ◽  
Preimplantation Genetic Diagnosis ◽  
Genetic Diagnosis ◽  
Indirect Linkage

scholarly journals Preimplantation genetic diagnosis for hemophilia A using indirect linkage analysis and direct genotyping approaches

2010 ◽  
Vol 8 (4) ◽  
pp. 783-789 ◽  
Author(s):  
A. D. LAURIE ◽  
A. M. HILL ◽  
J. R. HARRAWAY ◽  
A. P. FELLOWES ◽  
G. T. PHILLIPSON ◽  
...  
Keyword(s):  
Linkage Analysis ◽  
Preimplantation Genetic Diagnosis ◽  
Hemophilia A ◽  
Genetic Diagnosis ◽  
Indirect Linkage

scholarly journals Preimplantation Genetic Diagnosis of Neurodegenerative Diseases: Review of Methodologies and Report of Our Experience as a Regional Reference Laboratory

Diagnostics ◽  
2019 ◽  
Vol 9 (2) ◽  
pp. 44
Author(s):  
Liao ◽  
Chang ◽  
Ma ◽  
Chang ◽  
Lin ◽  
...  
Keyword(s):  
Linkage Analysis ◽  
Neurodegenerative Diseases ◽  
Embryo Transfer ◽  
Preimplantation Genetic Diagnosis ◽  
Quantitative Polymerase Chain Reaction ◽  
False Negative ◽  
Genetic Diagnosis ◽  
Oocyte Retrieval ◽  
Reference Laboratory ◽  
Inherited Disorders

Preimplantation genetic diagnosis (PGD) has become a crucial approach in helping carriers of inherited disorders to give birth to healthy offspring. In this study, we review PGD methodologies and explore the use of amplification refractory mutation system quantitative polymerase chain reaction (ARMS-qPCR) and/or linkage analysis for PGD in neurodegenerative diseases that are clinically relevant with typical features, such as late onset, and which are severely debilitating. A total of 13 oocyte retrieval cycles were conducted in 10 cases with various neurodegenerative diseases. Among the 59 embryos analyzed, 49.2% (29/59) were unaffected and 50.8% (30/59) were affected. Of the 12 embryo transfer cycles, three resulted in pregnancy, and all pregnancies were delivered. The implantation rate and livebirth rate were 23.1% (3/13) per oocyte retrieval cycle and 25.0% (3/12) per embryo transfer cycle. Allele dropout (ADO) was noted in two embryos that were classified as unaffected by ARMS-qPCR but were evidenced as affected after prenatal diagnosis, rendering the false negative rate as 6.3% (2/32). Four among the 13 cycles underwent PGD by ARMS-qPCR coupled with linkage analysis, and all were correctly diagnosed. We conclude that PGD by ARMS-qPCR and/or linkage analysis is a feasible strategy, whereas ADO is a concern when ARMS-qPCR is used as the sole technology in PGD, especially in autosomal dominant diseases.

Increased enquiries for preimplantation genetic diagnosis (PGD)

2014 ◽  
Vol 74 (S 01) ◽  
Author(s):  
KJ Heiliger ◽  
D Gutknecht ◽  
C Adelfalk ◽  
A Eder ◽  
M Bals-Pratsch ◽  
...  
Keyword(s):  
Preimplantation Genetic Diagnosis ◽  
Genetic Diagnosis
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