Genetic analysis of Turner syndrome in Tunisian patients: from diagnosis to management

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...

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Bibliographic Details
Main Authors: Olfa Siala-Sahnoun, Fatma Laadhar, Mouna Mnif, Wajdi Sefi, Faten Hadj Kacem, Mohamed A Kessentini, Mohamed Abid, Faiza Fakhfakh
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2023-01-01
Series:Journal of the Arab Society for Medical Research
Subjects:
epigenetic
genotype–phenotype correlation
karyotype
turner syndrome
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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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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