Genetic analysis of Turner syndrome in Tunisian patients: from diagnosis to management
Background/aim Turner syndrome (TS) is a rare sex chromosome abnormality in women, occurring in approximately one in 2500 live births, associated with a wide range of clinical stigmata of which short stature, ovarian dysgenesis, and dysmorphic features are the most frequent. Morbidity and mortality...
Main Authors: | Olfa Siala-Sahnoun, Fatma Laadhar, Mouna Mnif, Wajdi Sefi, Faten Hadj Kacem, Mohamed A Kessentini, Mohamed Abid, Faiza Fakhfakh |
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Format: | Article |
Language: | English |
Published: |
Wolters Kluwer Medknow Publications
2023-01-01
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Series: | Journal of the Arab Society for Medical Research |
Subjects: | |
Online Access: | http://www.new.asmr.eg.net/article.asp?issn=1687-4293;year=2023;volume=18;issue=1;spage=68;epage=75;aulast=Siala-Sahnoun |
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