Carlson, M. & Silberbach, M. Dissection of the aorta in Turner syndrome: two cases and review of 85 cases in the literature. Gene expression analysis of induced pluripotent stem cells from aneuploid chromosomal syndromes. These visits are an opportunity for the doctor to take height measurements, note delays in expected growth and identify other problems in physical development.If your family doctor or pediatrician believes that your child shows signs or symptoms of Turner syndrome and suggests diagnostic tests, you may want to ask these questions:Mayo Clinic does not endorse companies or products. The risk of hypertension is increased three-fold in patients with Turner syndrome. Bianchi, D. W. Turner syndrome: new insights from prenatal genomics and transcriptomics. Indeed, several studies had suggested an increased risk for aortic dissection in pregnancy.Recurrent acute otitis media (AOM) and otitis media with effusion (OME) commonly occur in children with Turner syndrome during the preschool age, which can persist or develop later in childhood. Turner syndrome can affect:1 DNA methylation signature in peripheral blood reveals distinct characteristics of human X chromosome numerical aberrations. Coronary calcification in adults with Turner syndrome.

Cardiovascular imaging in Turner syndrome: state-of-the-art practice across the lifespan. Sexual function in women with Turner syndrome. The importance of estrogen replacement in young women with Turner syndrome. Nature Reviews Endocrinology They are tall and thin, with long legs (see Chapters 16 and 17 Chapter 16 Chapter 17). Raznahan, A. et al. Schoemaker, M. J., Swerdlow, A. J., Higgins, C. D., Wright, A. F. & Jacobs, P. A. Mortality in women with Turner syndrome in Great Britain: a national cohort study. Naqvi, S., Bellott, D. W., Lin, K. S. & Page, D. C. Conserved microRNA targeting reveals preexisting gene dosage sensitivities that shaped amniote sex chromosome evolution.

Liver biochemical abnormalities in Turner syndrome: a comprehensive characterization of an adult population. In childhood, a short stature can be indicative of Turner syndrome.As a chromosomal condition, there is no cure for Turner syndrome. The abnormal cells may have only one X (In the majority of cases where monosomy occurs, the X chromosome comes from the mother.In most cases, Turner syndrome is a sporadic event, and for the parents of an individual with Turner syndrome the risk of recurrence is not increased for subsequent pregnancies.

You can also search for this author in Tanaka, T. et al. Patients with Turner syndrome are at risk of congenital heart defects (e.g., coarctation of aorta, bicuspid aortic valve) and may have progressive aortic root dilatation or dissection. All rights reserved. Otologic disorders in Turner syndrome. 3D genomic regulation of lncRNA and Xist in X chromosome. Andersen, N. H. et al. Bakalov, V. K. et al. Most girls and women have two complete X chromosomes (the sex chromosomes for females). Turner Syndrome (TS) is a condition that affects only girls and women. Prakash, S. K. et al. Gravholt, C. H., Naeraa, R. W., Fisker, S. & Christiansen, J. S. Body composition and physical fitness are major determinants of the growth hormone-insulin-like growth axis aberrations in adult Turner’s syndrome, with important modulations by treatment with 17β-estradiol. Estrogen replacement in Turner syndrome: literature review and practical considerations. Hong D, Scaletta Kent J, Kesler S. Cognitive profile of Turner syndrome. Vascular involvement of the liver in Turner’s syndrome. Mosaic Turner syndrome shows reduced penetrance in an adult population study. Increased fracture rates in Turner’s syndrome: a nationwide questionnaire survey. Research reported in 1997 noted that the karyotype can have a significant effect on the growth of children with Turner syndrome. Cintron, D. et al. & Castelo-Branco, C. Turner’s syndrome and other forms of congenital hypogonadism impair quality of life and sexual function. Doswell BH, Visootsak J, Brady AN, Graham JM Jr. Turner syndrome: an update and review for the primary pediatrician. J Clin Endocrinol Metab. In the meantime, to ensure continued support, we are displaying the site without styles Quigley, C. A. et al. and N.H.A. Taboada, M. et al. New issues in the diagnosis and management of Turner syndrome. Hagman, A. et al. researched data for the article, made substantial contributions to discussions of the content and wrote the article. Gravholt, C. H., Poulsen, H. E., Ott, P., Christiansen, J. S. & Vilstrup, H. Quantitative liver functions in Turner syndrome with and without hormone replacement therapy. Increased aortic stiffness in prepubertal girls with Turner syndrome. Yan, F., Wang, X. Another less common genetic pattern for Turner Syndrome (35%) is a mosaic.

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