Combination of Gonadal Dysgenesis and Monosomy X with a Novo Translocation (13,14)
Joint Authors
Latrech, Hanane
Gaouzi, Ahmed
Madar, Houssein
Source
Issue
Vol. 2018, Issue 2018 (31 Dec. 2018), pp.1-3, 3 p.
Publisher
Hindawi Publishing Corporation
Publication Date
2018-12-17
Country of Publication
Egypt
No. of Pages
3
Main Subjects
Abstract EN
Turner syndrome is a common sex chromosome disorder characterized by complete or partial absence of an X chromosome.
The spectrum of its clinical features and cytogenetics are various.
We report new chromosomal formula revealed by DSD and associated with translocation (13,14).
To our knowledge, this is the first case of 45X, t(13;14) de novo translocation as a variation of Turner syndrome in a patient with this clinical presentation.
American Psychological Association (APA)
Latrech, Hanane& Madar, Houssein& Gaouzi, Ahmed. 2018. Combination of Gonadal Dysgenesis and Monosomy X with a Novo Translocation (13,14). Case Reports in Endocrinology،Vol. 2018, no. 2018, pp.1-3.
https://search.emarefa.net/detail/BIM-1142943
Modern Language Association (MLA)
Latrech, Hanane…[et al.]. Combination of Gonadal Dysgenesis and Monosomy X with a Novo Translocation (13,14). Case Reports in Endocrinology No. 2018 (2018), pp.1-3.
https://search.emarefa.net/detail/BIM-1142943
American Medical Association (AMA)
Latrech, Hanane& Madar, Houssein& Gaouzi, Ahmed. Combination of Gonadal Dysgenesis and Monosomy X with a Novo Translocation (13,14). Case Reports in Endocrinology. 2018. Vol. 2018, no. 2018, pp.1-3.
https://search.emarefa.net/detail/BIM-1142943
Data Type
Journal Articles
Language
English
Notes
Includes bibliographical references
Record ID
BIM-1142943
