scholarly journals Natural transmission of a partial AZFb deletion of the Y chromosome over three generations: Case report

2002 ◽  
Vol 17 (9) ◽  
pp. 2267-2271 ◽  
Author(s):  
C. Rolf
Keyword(s):  
Case Report ◽  
Y Chromosome ◽  
Three Generations

Case report familial thrombocytopenia in seven members of three generations

1978 ◽  
Vol 63 (6) ◽  
pp. 136-141 ◽  
Author(s):  
Ivan P. Law ◽  
Andras Deveny ◽  
R. J. Meiser
Keyword(s):  
Case Report ◽  
Three Generations

Complete Azoospermia Factor b Deletion of Y Chromosome in an Infertile Male With Severe Oligoasthenozoospermia: Case Report and Literature Review

Urology ◽  
2017 ◽  
Vol 102 ◽  
pp. 111-115 ◽  
Author(s):  
Yong-Sheng Zhang ◽  
Lin-Lin Li ◽  
Lin-Tao Xue ◽  
Hao Zhang ◽  
Yue-Ying Zhu ◽  
...  
Keyword(s):  
Case Report ◽  
Literature Review ◽  
Y Chromosome ◽  
Infertile Male ◽  
Factor B ◽  
Azoospermia Factor

De novo Structure Variations of the Y Chromosome in a 47,XXY Female with Ovarian Failure: A Case Report

2014 ◽  
Vol 143 (4) ◽  
pp. 221-224 ◽  
Author(s):  
Bin Lin ◽  
Fengqin Tan ◽  
Heng Xu ◽  
Ping Wang ◽  
Quan Tang ◽  
...  
Keyword(s):  
Case Report ◽  
Y Chromosome ◽  
De Novo ◽  
Ovarian Failure

scholarly journals A CASE REPORT OF GARDNER'S SYNDROME WITH A FAMILY LINE SUFFERING FROM VARIOUS INTESTINAL DISEASES OVER THREE GENERATIONS

1986 ◽  
Vol 47 (12) ◽  
pp. 1628-1633
Author(s):  
Takashi HORIE ◽  
Haruhiko NAITO ◽  
Tsuyoshi TAKAHASHI ◽  
Kenji YAMAMOTO ◽  
Toshihiko TSUBURAYA ◽  
...  
Keyword(s):  
Case Report ◽  
Gardner's Syndrome ◽  
Gardner’S Syndrome ◽  
Intestinal Diseases ◽  
Three Generations

Usefulness of imprint cytology of gonadoblastoma with dysgerminoma in a patient with Turner syndrome and a Y chromosome: A case report and literature review

2019 ◽  
Vol 47 (11) ◽  
pp. 1203-1207
Author(s):  
Tamiko Nagai ◽  
Kiyoshi Hasegawa ◽  
Emi Motegi ◽  
Hiromi Machida ◽  
Hideo Sasaki ◽  
...  
Keyword(s):  
Case Report ◽  
Literature Review ◽  
Turner Syndrome ◽  
Y Chromosome ◽  
Imprint Cytology

47, XYY Syndrome and its Association with Male Infertility: Case Report

2020 ◽  
Vol 5 (04) ◽  
Author(s):  
Dr. Soni Ashish Kumar ◽  
Dr. Reddy Sanjeeva N
Keyword(s):  
Case Report ◽  
Male Infertility ◽  
Y Chromosome ◽  
Chorionic Gonadotropin ◽  
Peripheral Blood Lymphocytes ◽  
Severe Oligozoospermia ◽  
Early Management ◽  
Conventional Cytogenetic Analysis ◽  
Infertile Men ◽  
Xyy Syndrome

47, XYY syndrome is one of the most common sex chromosomal anomaly found in humans after Klinfelter syndrome (47, XXY). It is frequently associated with infertility in males. This syndrome has an extra Y chromosome (XYY) due to non-disjunction of the Y chromosome in paternal meiotic II. The presence of an extra Y chromosome causes hormonal disbalance in the gonads that responsible for abnormal function of human chorionic gonadotropin. In our case of infertile men with severe oligozoospermia that also confirm by conventional cytogenetic analysis of the peripheral blood lymphocytes revealed the constitutional karyotype of 47, XYY. This report is likely to be helpful for counselling and early management of such infertile males.

Significance of Y Chromosome in a Turner Mosaic Girl with Dysgerminoma: Case Report with Literature Review

2021 ◽  
Vol 19 (4) ◽  
Author(s):  
R. N. Abinaya ◽  
P. Rema ◽  
S. Suchetha ◽  
J. Sivaranjith ◽  
Dhanya Dinesh
Keyword(s):  
Case Report ◽  
Literature Review ◽  
Y Chromosome

scholarly journals Novel Y chromosome breakpoint in an infertile male with a de novo translocation t(Y;16): a case report

2012 ◽  
Vol 29 (12) ◽  
pp. 1427-1430 ◽  
Author(s):  
Yu-Ting Jiang ◽  
Hong-Guo Zhang ◽  
Rui-Xue Wang ◽  
Yang Yu ◽  
Zhi-Hong Zhang ◽  
...  
Keyword(s):  
Case Report ◽  
Y Chromosome ◽  
De Novo ◽  
Infertile Male ◽  
Chromosome Breakpoint ◽  
De Novo Translocation
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