scholarly journals Extra G Positive Band on Long Arm of Chromosome 9 and Long Y-Chromosome in a Patient Presenting with Infertility: A Case Report

Author(s):  
Afreen Aftab ◽  
Kundavi Shankar ◽  
Bibhas Kar
Urology ◽  
2017 ◽  
Vol 102 ◽  
pp. 111-115 ◽  
Author(s):  
Yong-Sheng Zhang ◽  
Lin-Lin Li ◽  
Lin-Tao Xue ◽  
Hao Zhang ◽  
Yue-Ying Zhu ◽  
...  

2013 ◽  
Vol 161 (6) ◽  
pp. 1447-1452 ◽  
Author(s):  
Else la Cour Sibbesen ◽  
Cathrine Jespersgaard ◽  
Daniela Alosi ◽  
Anne-Marie Bisgaard ◽  
Zeynep Tümer

2014 ◽  
Vol 143 (4) ◽  
pp. 221-224 ◽  
Author(s):  
Bin Lin ◽  
Fengqin Tan ◽  
Heng Xu ◽  
Ping Wang ◽  
Quan Tang ◽  
...  

2019 ◽  
Vol 47 (11) ◽  
pp. 1203-1207
Author(s):  
Tamiko Nagai ◽  
Kiyoshi Hasegawa ◽  
Emi Motegi ◽  
Hiromi Machida ◽  
Hideo Sasaki ◽  
...  

2019 ◽  
Vol 7 ◽  
pp. 2050313X1982963
Author(s):  
Joanna Yuen ◽  
Fatmah AlZahrani ◽  
Garnet Horne ◽  
Karen Naert ◽  
Timothy McCalmont ◽  
...  

Atypical Spitzoid lesions pose a distinct challenge in classification as they may comprise a mixture of both classic benign nevus and cutaneous melanoma characteristics. Immunostaining and molecular analysis, such as comparative genomic hybridization, can assist in narrowing the differential diagnosis. We present a case of a 5-year-old male with an atypical Spitzoid lesion on his back. Initial histopathology revealed a relatively symmetric lesion with mitotic figures and poor maturation of melanocytes with descent into the dermis. Immunohistochemistry demonstrated a loss of p16, and array comparative genomic hybridization revealed a loss of chromosome 9, supporting a diagnosis of invasive melanoma arising in conjunction with a remnant of a conventional melanocytic nevus. This case is the first in Canada to demonstrate the use of array comparative genomic hybridization for diagnosing melanoma in a young paediatric patient.


Author(s):  
Dr. Soni Ashish Kumar ◽  
Dr. Reddy Sanjeeva N

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.


2021 ◽  
Vol 19 (4) ◽  
Author(s):  
R. N. Abinaya ◽  
P. Rema ◽  
S. Suchetha ◽  
J. Sivaranjith ◽  
Dhanya Dinesh

2012 ◽  
Vol 29 (12) ◽  
pp. 1427-1430 ◽  
Author(s):  
Yu-Ting Jiang ◽  
Hong-Guo Zhang ◽  
Rui-Xue Wang ◽  
Yang Yu ◽  
Zhi-Hong Zhang ◽  
...  

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