نتایج جستجو برای: turner

تعداد نتایج: 6209  

2017

Turner's syndrome is a genetic disorder that affects only females. Turner syndrome is caused by a chromosomal abnormality in which all or part of one of the X chromosomes is missing or altered. While most people have 46 chromosomes, people with TS usually only have 45. This condition occurs in about 1 out in 2,500 female live births worldwide (but it is much more common among miscarriages and s...

Journal: :Journal of American Studies 2015

2017

Turner's syndrome is a genetic disorder that affects only females. Turner syndrome is caused by a chromosomal abnormality in which all or part of one of the X chromosomes is missing or altered. While most people have 46 chromosomes, people with TS usually only have 45. This condition occurs in about 1 out in 2,500 female live births worldwide (but it is much more common among miscarriages and s...

2009
Frederick Jackson Turner Frederick Jackson

During a gathering ofhistorians at the World’s Columbian Exhibition in Chicago in 1893, Frederick Jackson Turner presented an essay titled “The Sign Ulcance of the Frontier in American Histoiy. “ Turner ‘s article, also known as the Frontier Thesis, argued that the settlement ofthe frontier made the American nation unique. Turner credited the frontier’s settlement as the primaryforce in shaping...

2017

Turner's syndrome is a genetic disorder that affects only females. Turner syndrome is caused by a chromosomal abnormality in which all or part of one of the X chromosomes is missing or altered. While most people have 46 chromosomes, people with TS usually only have 45. This condition occurs in about 1 out in 2,500 female live births worldwide (but it is much more common among miscarriages and s...

2017

Turner's syndrome is a genetic disorder that affects only females. Turner syndrome is caused by a chromosomal abnormality in which all or part of one of the X chromosomes is missing or altered. While most people have 46 chromosomes, people with TS usually only have 45. This condition occurs in about 1 out in 2,500 female live births worldwide (but it is much more common among miscarriages and s...

2017
Daniel G. H. Devos Katya De Groote Danilo Babin Laurent Demulier Yves Taeymans Jos J. Westenberg Luc Van Bortel Patrick Segers Eric Achten Jean De Schepper Ernst Rietzschel

BACKGROUND To study segmental structural and functional aortic properties in Turner syndrome (TS) patients. Aortic abnormalities contribute to increased morbidity and mortality of women with Turner syndrome. Cardiovascular magnetic resonance (CMR) allows segmental study of aortic elastic properties. METHOD We performed Pulse Wave Velocity (PWV) and distensibility measurements using CMR of the...

2013
Christian Trolle Kristian H. Mortensen Lisbeth N. Pedersen Agnethe Berglund Henrik K. Jensen Niels H. Andersen Claus H. Gravholt

OBJECTIVES 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 Turner syndrome phenotype. METHODS Adult women with Turner syndrome (n = 88) were examined thrice and 68 age-matched healthy contro...

Journal: :Indian pediatrics 2015
Deep Dutta Chitra Selvan Satinath Mukhopadhyay

BACKGROUND Multiple pituitary hormone deficiency and Turner syndrome have overlapping features in peripubertal girls and is a diagnostic challenge. CASE CHARACTERISTICS 16-year-old girl having Turner phenotype undergoing evaluation for severe short stature and pubertal arrest. OBSERVATION 45,X karyotype, and multiple pituitary hormone deficiency with empty sella. INTERVENTION Levothyroxin...

2014
Kai-Ming Jhang Tung-Ming Chang Ming Chen Chin-San Liu

INTRODUCTION Reports on cases of epilepsy in Turner syndrome are rare and most of them have cortical developmental malformations. We report the case of a Taiwanese patient with mosaic Turner syndrome with generalized tonic-clonic epilepsy and asymmetrical lateral ventricles but no apparent cortical anomaly. CASE PRESENTATION A 49-year-old Taiwanese woman without family history presented with ...

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