Transsexualism in a Klinefelter male: a case report

1992 ◽  
Vol 9 (1) ◽  
pp. 45-46 ◽  
Author(s):  
Elizabeth M J Cryan ◽  
Frank P O'Donoghue

AbstractWe report a Klinefelter male who presents requesting gender reassignment surgery. There may be a predisposition to gender dysphoria in Klinefelter's Syndrome, and in the case we describe, the perception of his symptoms as being of biological origin coupled with the unavailability of gender reassignment surgery in the Republic of Ireland has had a negative therapeutic effect.

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.


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

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.


2018 ◽  
Vol 79 (2) ◽  
pp. 314-338 ◽  
Author(s):  
David Albert Jones

There is no explicit authoritative Catholic teaching on gender reassignment surgery (GRS). Catholic bioethicists have debated the origin of gender dysphoria and the effectiveness of GRS. A further ethical question is whether some forms of GRS involve “mutilation in the strict sense.” The principle of totality does not apply to GRS as the reproductive organs are a cause of distress only because the object of distress. This analysis leaves open the status of GRS which does not compromise biological function.


Sign in / Sign up

Export Citation Format

Share Document