Results 1 to 10 of about 51,939 (308)
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
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
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
doaj +1 more source
PLoS ONE, 2020 Individuals with Mathematics Learning Disabilities have persistent mathematics underperformance but vary with respect to their cognitive profiles.
Sarah L. Lukowski +7 more
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A case of duplication of inferior vena cava and turner syndrome: Is it a rare association?
Indian Journal of Vascular and Endovascular Surgery, 2022 Turner syndrome is one of the most common sex chromosome disorders with many anatomical abnormalities that affect physiological systems of human body. The most common cardiovascular anomalies in Turner syndrome are bicuspid aortic valve and coarctation ...
S BS Netam +3 more
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Long QT interval in Turner syndrome--a high prevalence of LQTS gene mutations. [PDF]
PLoS ONE, 2013 QT-interval prolongation of unknown aetiology is common in Turner syndrome. This study set out to explore the presence of known long QT mutations in Turner syndrome and to examine the corrected QT-interval (QTc) over time and relate the findings to the ...
Christian Trolle +6 more
doaj +1 more source
Mosaic Turner syndrome associated with schizophrenia [PDF]
Annals of Pediatric Endocrinology & Metabolism, 2014 Turner syndrome is a sex-chromosome disorder; occurring in 1 in 2,500 female births. There are sporadic few case reports of concomitant Turner syndrome with schizophrenia worldwide.
Sook Young Jung +5 more
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A single-center's uric acid profile in girls with Turner syndrome. [PDF]
Front Endocrinol (Lausanne)Guo S +8 more
europepmc +3 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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Cardiovascular Disease and Inpatient Complications in Turner Syndrome: A Propensity Score Analysis [PDF]
Texas Heart Institute JournalBackground Turner syndrome is a genetic disorder that occurs in female individuals and is characterized by the absence of 1 of the X chromosomes. This study examined the risk of cardiovascular disease and inpatient clinical outcomes in patients with ...
Talal Alzahrani, MD, MPH
doaj +1 more source