Cardiac abnormalities in girls with Turner syndrome: ECG abnormalities, myocardial strain imaging, and karyotype–phenotype associations
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چکیده
منابع مشابه
Relationship between Baseline ECG Abnormalities and Quantitative Perfusion Parameters of Myocardial Perfusion Findings
Background: Coronary Artery Disease (CAD) is one of the major causes of mortality in most countries. Electrocardiography (ECG) and myocardial perfusion imaging (MPI) are non-invasive disgnostic tests for CAD. Finding a relationship between abnormal findings in the baseline ECG and MPI findings can be helpful in better diagnosis of CAD. Materials and Methods: The present study examined ECG of pa...
متن کامل[Cardiac abnormalities in LEOPARD syndrome].
LEOPARD syndrome is an autosomal dominant genetic disorder involving a complex of malformations and other features, including lentiginosis, electrocardiographic conduction abnormalities, ocular hypertelorism, pulmonary valve stenosis, abnormal genitalia, growth retardation, and sensorineural deafness. The most common cardiovascular manifestations of this condition are pulmonary valve stenosis, ...
متن کاملEarly metabolic abnormalities in adolescent girls with polycystic ovarian syndrome.
OBJECTIVE To investigate insulin sensitivity and secretion in young adolescent girls with childhood onset polycystic ovarian syndrome (PCOS) and to identify the early metabolic derangement(s). STUDY DESIGN Twelve obese girls with PCOS (age 12.0+/-0.7 years) were compared with 10 obese nonhyperandrogenic girls (control group). The groups were matched for age, percent body fat, and abdominal fa...
متن کاملecg abnormalities in rural areas
a survey was carried out in the summer of 1972 in east azerbaijan, northwest iran, to determine the prevalence of cardiovascular disease. ecg tracings were prepared from 198 women and 178 men aged 40-60. only 45% of the tracings were completely normal. q/qs abnormalities were found in 4.7% of tracings, left axis deviation in 4% tall r wave in 37%, st depression in 3.9% of men and 14.1% of women...
متن کاملWhite matter microstructural abnormalities in girls with chromosome 22q11.2 deletion syndrome, Fragile X or Turner syndrome as evidenced by diffusion tensor imaging
Children with chromosome 22q11.2 deletion syndrome (22q11.2DS), Fragile X syndrome (FXS), or Turner syndrome (TS) are considered to belong to distinct genetic groups, as each disorder is caused by separate genetic alterations. Even so, they have similar cognitive and behavioral dysfunctions, particularly in visuospatial and numerical abilities. To assess evidence for common underlying neural mi...
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ژورنال
عنوان ژورنال: American Journal of Medical Genetics Part A
سال: 2021
ISSN: 1552-4825,1552-4833
DOI: 10.1002/ajmg.a.62259