scholarly journals P-25 Birth of a healthy boy from a patient with nonmosaic Klinefelter's syndrome after IVF-ICSI with preimplantation genetic diagnosis (PGD) – Case report

2013 ◽  
Vol 26 ◽  
pp. S36-S37
Author(s):  
G. Mskhalaya ◽  
E. Zakharova ◽  
M. Potapov ◽  
V. Zaletova ◽  
E. Efremov
2003 ◽  
Vol 7 (3) ◽  
pp. 346-352 ◽  
Author(s):  
S Kahraman ◽  
N Findikli ◽  
H Berkil ◽  
E Bakircioglu ◽  
E Donmez ◽  
...  

2019 ◽  
Vol 20 (1) ◽  
Author(s):  
Dan Li ◽  
Yun Wang ◽  
Nan Zhao ◽  
Liang Chang ◽  
Ping Liu ◽  
...  

Abstract Background Uniparental disomy (UPD) refers to the situation in which two copies of homologous chromosomes or part of a chromosome originate from the one parent and no copy is supplied by the other parent. Case presentation Here, we reported a woman whose karyotype was 46, XX, t (1;17)(q42;q21), has obtained 5 embryos by intracytoplasmic sperm injection (ICSI) after one cycle of in vitro fertility (IVF). After microarray-based comparative genomic hybridization (array-CGH) for preimplantation genetic testing for chromosomal structural rearrangements (PGT-SR), two embryos were balanced, one balanced embryo was implanted and the patient successfully achieved pregnancy. Amniocentesis was performed at the 19th week of gestation for karyotype analysis and single nucleotide polymorphism (SNP)-array test. The result of karyotype analysis was: mos 47, XXY [19]/46, XY [81]; SNP-array results revealed 46, XY, iUPD (9) pat. After full genetic counseling for mosaic Klinefelter’s syndrome and paternal iUPD (9), the couple decided to continue pregnancy, and the patient gave birth to a healthy boy. The newborn is now 3.5 years old, and developed normally. This case will provide counseling evidences of paternal iUPD (9) for doctors. Conclusions This is the first case report of paternal iUPD9 with mosaic Klinefelter’s syndrome, and no abnormality has been observed during the 3.5-year follow-up. Further observation is required to determine whether the imprinted genes on the chromosomes are pathogenic and whether recessive pathogenetic genes are activated.


2010 ◽  
Vol 21 (5) ◽  
pp. 658-662 ◽  
Author(s):  
Rosa Bautista-Llácer ◽  
Trinitat M. Alberola ◽  
Xavier Vendrell ◽  
Esther Fernández ◽  
Manuel Pérez-Alonso

1996 ◽  
Vol 19 (4) ◽  
pp. 248-252 ◽  
Author(s):  
Ana Claudia de A. R. Pinto ◽  
M. A. Czepielewski ◽  
J. L. Gross ◽  
W. Mussio ◽  
A. M. J. Lengyel

2005 ◽  
Vol 20 (3) ◽  
pp. 697-701 ◽  
Author(s):  
S.K.M. Seeho ◽  
G. Burton ◽  
D. Leigh ◽  
J.T. Marshall ◽  
J.W. Persson ◽  
...  

1981 ◽  
Vol 26 (4) ◽  
pp. 262-264 ◽  
Author(s):  
Alec Roy

Psychiatric disorder in relation to Klinefelter's syndrome is reviewed. A well documented case report is presented of a schizophreniform illness in a patient with Klinefelter's.


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