Results 1 to 10 of about 1,421,602 (199)
Long QT interval in Turner syndrome--a high prevalence of LQTS gene mutations. [PDF]
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 +3 more sources
Mosaic Turner syndrome associated with schizophrenia [PDF]
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
doaj +2 more sources
A Review of Recent Developments in Turner Syndrome Research
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
doaj +3 more sources
A Rare Variant of Turner Syndrome (the X Isochromosome-X Syndrome): A Case Report [PDF]
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
Individuals with Mathematics Learning Disabilities have persistent mathematics underperformance but vary with respect to their cognitive profiles.
Sarah L. Lukowski +7 more
doaj +2 more sources
A case of duplication of inferior vena cava and turner syndrome: Is it a rare association?
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
doaj +1 more source
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
doaj +1 more source
Cardiovascular Disease and Inpatient Complications in Turner Syndrome: A Propensity Score Analysis [PDF]
Background 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
An Automated Approach to Diagnose Turner Syndrome Using Ensemble Learning Methods
This research proposes to use ensemble learning methods to diagnose and predict Turner syndrome using facial images. Turner syndrome, also known as congenital ovarian hypoplasia syndrome, is a common clinical chromosomal disorder.
Qing Zhao +4 more
doaj +1 more source
Pathology of the Cardiovascular System in Children with Turner Syndrome
The paper studies the structure of the pathology of the cardiovascular system in children with Turner syndrome. The results of the survey are based on the findings from 42 patients with Turner syndrome, aged 1.5 to 17 years. It is shown that in 80.9 % of
A.Ye. Abaturov +3 more
doaj +1 more source

