turner syndrome patient
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2020 ◽  
Vol 2020 (10) ◽  
Author(s):  
D A Chávez-Fernández ◽  
E Zúñiga-Garza ◽  
R A López-Saucedo

Abstract We report a case of primary tracheal schwannoma in a 31-year-old woman. She had a previous history of follicular thyroid carcinoma treated surgically and Turner syndrome. In a follow-up computed tomography scan, we found a partially obstructing intraluminal tracheal tumor, which was confirmed by bronchoscopy. The patient was treated by surgical resection and primary tracheal anastomosis. The tumor was 14 mm in diameter, with an intact capsule. Histologic analysis revealed a Schwann cell origin tumor.


2020 ◽  
Vol 49 (3) ◽  
pp. 102-105
Author(s):  
Shintaro Takago ◽  
Hiroki Kato ◽  
Naoki Saito ◽  
Hideyasu Ueda ◽  
Kenji Iino ◽  
...  

2018 ◽  
Vol 31 (3) ◽  
pp. 349-353 ◽  
Author(s):  
Ruen Yao ◽  
Ding Yu ◽  
Jian Wang ◽  
Xiumin Wang ◽  
Yiping Shen

AbstractBackground:Y:autosome translocations are reported to be associated with male infertility and azoospermia. Female cases with Y:autosome translocation are extremely rare.Case presentation:We report a unique case of a rare unbalanced translocation t(Y;13) in a 12-year-old girl with Turner syndrome. Combined cytogenetic testing helped to demonstrate the detail of rare chromosomal structural rearrangement in this patient.Conclusions:The presented case showed femaleness phenotype and failure of masculinization with presence of Y chromosome and theSRYgene. She was treated with growth hormone (GH) therapy after confirming the presence of only female internal gonad with laparoscopy.


2016 ◽  
Vol 62 (1) ◽  
pp. 77-83 ◽  
Author(s):  
Rasime Kalkan ◽  
Nermin Özdağ ◽  
Rüveyde Bundak ◽  
Ayşe Çirakoğlu ◽  
Nedime Serakinci

2015 ◽  
Vol 1 (2) ◽  
pp. e105-e110
Author(s):  
Xiang Wang ◽  
Minggang Zhao ◽  
Wei Chen ◽  
Fang He ◽  
Wenfang Yang ◽  
...  

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