2019 ◽  
Author(s):  
Hela Marmouch ◽  
Haythem Jenzri ◽  
Houssem Mrabet ◽  
Hamza Fekih ◽  
Ines Khochtali

2014 ◽  
Author(s):  
Robert I McLachlan ◽  
Andrew N Stephens ◽  
Adam Rainczuk ◽  
Caroline Foo ◽  
Mark R Condina ◽  
...  

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.


CHEST Journal ◽  
1982 ◽  
Vol 82 (1) ◽  
pp. 132 ◽  
Author(s):  
Basil Varkey ◽  
Akira Funahashi

1987 ◽  
Vol 24 (7) ◽  
pp. 439-441 ◽  
Author(s):  
A D Ormerod ◽  
M I White ◽  
E McKay ◽  
A W Johnston

1981 ◽  
Vol 26 (8) ◽  
pp. 567-568 ◽  
Author(s):  
V.K. Yeragani ◽  
G. Hopkinson

The authors thought it would be of interest to present this case which proved to be Klinefelter's syndrome with “xxy” pattern, as the patient presented with episodes of abnormal behaviour lasting for a few minutes. He would suddenly become anxious, look perplexed, start clenching his fists and at times complain of thoughts that some persons were trying to attack him. He also felt as if he were hearing voices talking to him. Observation in the hospital and EEG recording helped to rule out temporal lobe epilepsy and a diagnosis of Klinefelter's syndrome with personality disorder and psychogenic attacks of abnormal behaviour was made at the time of discharge.


1987 ◽  
Vol 151 (3) ◽  
pp. 398-400 ◽  
Author(s):  
J. Raboch ◽  
H. Černá ◽  
P. Zemek

Male sex hormones are ascribed a great importance in the literature from the point of view of sexual activity and aggressive behaviour. Two cases of sexually motivated murder are described, committed by delinquents with low levels of testosterone in plasma: one a patient with Klinefelter's syndrome; the other a man after castration. Even a decreased level of androgens, either primary or secondary, is not an absolute prevention of sexually aggressive behaviour.


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