Sex Chromosome Variations: Klinefelter's Syndrome

Intersex ◽  
2020 ◽  
pp. 143-169
Author(s):  
Catherine Harper
1974 ◽  
Vol 125 (586) ◽  
pp. 236-237 ◽  
Author(s):  
Johannes Nielsen ◽  
Takayuki Tsuboi

Previous electroencephalographic studies of persons with sex chromosome aberrations have indicated that there might be more electroencephalographic aberrations in males with double Y and double X than in the general population. A survey of these studies has recently been made by Fenton et al. (1971).


1998 ◽  
Vol 69 (3) ◽  
pp. 482-485 ◽  
Author(s):  
Roland Kruse M.D. ◽  
Martina Guttenbach Ph.D. ◽  
Bettina Schartmann M.Sc. ◽  
Regine Schubert Ph.D. ◽  
Hans van der Ven M.D. ◽  
...  

1988 ◽  
Vol 52 (2) ◽  
pp. 93-109 ◽  
Author(s):  
P. A. JACOBS ◽  
T. J. HASSOLD ◽  
E. WHITTINGTON ◽  
G. BUTLER ◽  
S. COLLYER ◽  
...  

2004 ◽  
Vol 47 (2) ◽  
pp. 163-175 ◽  
Author(s):  
Nouha Bouayed Abdelmoula ◽  
Ahlem Amouri ◽  
Marie-France Portnoi ◽  
Ali Saad ◽  
Tahia Boudawara ◽  
...  

1968 ◽  
Vol 17 (2) ◽  
pp. 385-388 ◽  
Author(s):  
Johannes Nielsen

SummaryA multiple birth frequency of 5.59% has been found in 25 Klinefelter sibships, which is statistically significantly higher than expected (P < 0.001).A family investigation of a patient with Klinefelter's syndrome, who is a triplet himself, revealed 5 twin births and 2 triplet births in three generations.The mortality of the 19 children from the 9 multiple births born in the 25 Klinefelter sibships was 53% up to the age of 3. Such a high mortality indicates that some of the twins and triplet births might have suffered from chromosome disorders contributing to the high mortality.If the comparatively high frequency of twins in the sibships with Klinefelter's syndrome as well as Turner's syndrome is confirmed by further studies, this will indicate a relation between the cause of sex chromosome non-disjunction and multiple births or between the predisposition to non-disjunction and multiple births.


1999 ◽  
Vol 84 (10) ◽  
pp. 3807-3810 ◽  
Author(s):  
Carlo Foresta ◽  
Carlo Galeazzi ◽  
Andrea Bettella ◽  
Paola Marin ◽  
Marco Rossato ◽  
...  

Abstract Azoospermic subjects affected by Klinefelter’s syndrome may occasionally show the presence of intratesticular residual foci of spermatogenesis, and the retrieval of mature spermatozoa from the testis may permit fertility and paternity by means of intracytoplasmic sperm injection. Previous studies have demonstrated that these subjects show the presence of an increased incidence of hyperaploid spermatozoa. Here we analyzed, by fluorescence in situ hybridization using specific probes for chromosomes 8, X, and Y, the spermatogenic process and the meiotic progression of 47,XXY germ cells retrieved by fine needle aspiration of the testis in ten azoospermic patients affected by classic Klinefelter’s syndrome. All patients had lower testicular volume, higher gonadotropins, and lower testosterone plasma levels compared with control subjects. Cytological analysis of the testicular cells retrieved by fine needle aspiration showed the presence of Sertoli cells only in eight subjects, while germ cells were observed in two patients. In each patient Sertoli cells showed a 47,XXY karyotype, and the same chromosome pattern was observed in spermatogonia and primary spermatocytes of patients presenting a residual spermatogenesis. Secondary spermatocytes, spermatids, and mature spermatozoa showed different sex chromosome patterns, reflecting their origin from 47,XXY spermatogonia. In conclusion, this study demonstrated that, in subjects affected by Klinefelter’s syndrome, residual germ cells may be present in the testis and that 47,XXY spermatogonia are able to undergo and complete the spermatogenic process leading to mature spermatozoa. These data further suggest the need to evaluate the sex chromosome status of sperm from patients affected by Klinefelter’s syndrome undergoing assisted reproductive techniques.


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