Turner Syndrome and Its Variants
Turner syndrome (TS) is a genetic disorder which is characterized by the complete or partial absence of the X chromosome. The incidence is 1/2500 female live births. The main clinical findings are short stature, primary amenorrhea and infertility, and phenotypical features include webbed neck, a low...
Main Authors: | Semra Gürsoy, Derya Erçal |
---|---|
Format: | Article |
Language: | English |
Published: |
Galenos Yayinevi
2017-12-01
|
Series: | Journal of Pediatric Research |
Subjects: | |
Online Access: | http://jpedres.org/archives/archive-detail/article-preview/turner-syndrome-and-ts-variants/165062147-9445 |
Similar Items
-
Evaluating the relationship between the proportion of X-chromosome deletions and clinical manifestations in children with turner syndrome
by: Gaowei Wang, et al.
Published: (2024-02-01) -
Double isochromosome X, A rare cytogenetic variant of turner syndrome: A case report and a review of the literature
by: Zerrouki K., et al.
Published: (2023-03-01) -
A Rare Variant of Turner Syndrome (the X Isochromosome-X Syndrome): A Case Report
by: Hamid Reza Samimagham, et al.
Published: (2021-12-01) -
A rare case of mosaic ring turner syndrome with horseshoe kidney
by: Kumari Pritti, et al.
Published: (2022-01-01) -
A rare of Turner syndrome with a special karyotype: a case report
by: W.D. Huang, et al.
Published: (2020-02-01)