A basic understanding of Turner syndrome: Incidence, complications, diagnosis, and treatment

Author:

Cui Xiaoxiao12,Cui Yazhou2,Shi Liang2,Luan Jing2,Zhou Xiaoyan2,Han Jinxiang2

Affiliation:

1. School of Medicine and Life Sciences, University of Ji’nan-Shandong Academy of Medical Science

2. Key Laboratory for Rare Disease Research of Shandong Province, Key Laboratory for Biotech Drugs of the Ministry of Health, Shandong Medical Biotechnological Center, Shandong Academy of Medical Sciences

Publisher

International Research and Cooperation Association for Bio & Socio-Sciences Advancement (IRCA-BSSA)

Subject

General Medicine

Reference52 articles.

1. 1. Zhang F, Zhang Z. Advances in the study of the diagnosis and treatment of Turner syndrome. Journal of China-Japan Friendship Hospital. 2015; 29:192-194. (in Chinese)

2. 2. Ford CE, Jones KW, Polani PE, De Almeida JC, Briggs JH. A sex-chromosome anomaly in a case of gonadal dysgenesis (Turner's syndrome). Lancet. 1959; 1:711-713.

3. 3. WWolff DJ, Van Dyke DL, Powell CM, Working Group of the ACMG Laboratory Quality Assurance Committee. Laboratory guideline for Turner syndrome. Genet Med. 2010; 12:52-55.

4. 4. Baena N, De Vigan C, Cariati E, Clementi M, Stoll C, Caballín MR, Guitart M. Turner syndrome: Evaluation of prenatal diagnosis in 19 European registries. Am J Med Genet A. 2004; 15:16-20.

5. 5. Wang H, He Y, Shao X, Ding Y. Clinical characteristics and chromosome analysis of 67 children with Turner syndrome in Suzhou. Chinese Journal of Birth Health & Heredity. 2009; 17:52-53. (in Chinese)

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