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Child and Adolescent Psychiatric Clinics of North America, 2023 Turner syndrome is a neurogenetic disorder characterized by partial or complete monosomy-X. It is associated with certain physical and medical features, including estrogen deficiency, short stature, and increased risk for several diseases, with cardiac conditions being among the most serious.
S. Kesler
semanticscholar +3 more sources
Left Ventricular Noncompaction in a Child with Turner Syndrome [PDF]
Case Reports in Pediatrics, 2019 Congenital heart disease (CHD) may cause a significant comorbidity in patients with Turner syndrome. The commonly reported CHD in these patients includes bicuspid aortic valve and coarctation of the aorta.
Snigdha Bhatia +4 more
doaj +2 more sources
Journal of Neurodevelopmental Disorders, 2021 Background Turner syndrome is the result of the partial or complete absence of an X chromosome in phenotypic girls. This can cause an array of medical and developmental difficulties.
Hanna Björlin Avdic +6 more
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A Review of Recent Developments in Turner Syndrome Research
Journal of Cardiovascular Development and Disease, 2021 Turner syndrome is a rare disorder resulting from complete or partial loss of the second sex chromosome. Common manifestations include delayed growth, premature ovarian failure, congenital heart defects, endocrine disorders, lymphedema, and webbed neck ...
Allen C. Huang +2 more
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Cardiovascular Health in Turner Syndrome: A Scientific Statement From the American Heart Association
Circulation Genomic and Precision Medicine, 2018 Girls and women with Turner syndrome face a lifelong struggle with both congenital heart disease and acquired cardiovascular conditions. Bicuspid aortic valve is common, and many have left-sided heart obstructive disease of varying severity, from ...
Michael Silberbach +2 more
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Endocrines, 2022 Turner syndrome (TS) affects approximately 1 out of every 1500–2500 live female births, with clinical features including short stature, premature ovarian failure, dysmorphic features and other endocrine, skeletal, cardiovascular, renal, gastrointestinal ...
Ethel Gonzales Clemente +4 more
doaj +4 more sources
Estrogen Replacement in Turner Syndrome: Literature Review and Practical Considerations
Journal of Clinical Endocrinology and Metabolism, 2018 Robert L Rosenfield +2 more
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Parsonage Turner syndrome after COVID‐19 vaccination
Muscle and Nerve, 2021 1 | INTRODUCTION Parsonage Turner syndrome (PTS, brachial neuritis or neuralgic amyotrophy), is a clinical syndrome typically characterized by acute onset of unilateral severe pain in the shoulder and upper arm, followed by weakness in the proximal mid ...
Shalini Mahajan +3 more
semanticscholar +2 more sources
A Rare Variant of Turner Syndrome (the X Isochromosome-X Syndrome): A Case Report [PDF]
Disease and Diagnosis, 2021 Background: Turner syndrome occurs in nearly one in every 2000-5000 female births. This syndrome is a genetic problem in the female phenotype and the most common sex chromosome anomaly.
Hamid Reza Samimagham +1 more
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The Turner syndrome life course project: Karyotype‐phenotype analyses across the lifespan
Clinical Endocrinology, 2017 Antoinette Cameron-Pimblett +2 more
exaly +2 more sources