Turner Syndrome News and Research

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Turner syndrome affects approximately 1 out of every 2,500 female live births worldwide. It embraces a broad spectrum of features, from major heart defects to minor cosmetic issues. Some individuals with Turner syndrome may have only a few features, while others may have many. Almost all people with Turner syndrome have short stature and loss of ovarian function, but the severity of these problems varies considerably amongst individuals.

Genetic screening results just got harder to handle under new abortion rules

Ann was 15 weeks pregnant with her fourth child when the results of her prenatal genetic test came back last August.

27 Jun 2022

New mobile phone app could enable early identification of treatable growth disorders

A ground-breaking new, mobile phone app, 'GrowthMonitor' places the accurate measurement of children's height in the hands of parents and carers.

8 Nov 2021

Researchers report rare case of cardiac arrhythmias in a neonate with Turner syndrome

Doctors treating babies born with Turner syndrome need to look for heart rhythm abnormalities, in addition to the usual heart problems of high blood pressure or left-sided structural heart defects, according to Meena Bolourchi, MD, assistant professor of pediatrics at Boston University School of Medicine.

30 Apr 2021

Microsurgery improves outcomes in patients experiencing paralysis from Parsonage-Turner Syndrome

Orthopedic surgeons at Hospital for Special Surgery performed successful microsurgery to repair damaged nerves and restore muscle strength and movement to patients experiencing paralysis from Parsonage-Turner Syndrome, according to a study published online ahead of print in The Journal of Hand Surgery.

27 Oct 2020

HSS researchers use novel MRI technique to study Parsonage-Turner Syndrome

Researchers at Hospital for Special Surgery (HSS) have received a grant from the National Institutes of Health to use a novel MRI technique known as magnetic resonance neurography, or MRN, to study Parsonage-Turner Syndrome (PTS), a painful nerve disorder that leads to severe weakness.

24 Sep 2020

MGH researchers identify key mechanism in X chromosome inactivation

Researchers at Massachusetts General Hospital have identified a key mechanism in X chromosome inactivation, a phenomenon that may hold clues that lead to treatments for certain rare congenital disorders.

12 Jun 2020

Cardiovascular surgeons heal a patient’s aortic dissection

When James Inman, 59, first experienced chest pain one night, he tried to brush it off and go back to sleep. But the pain became unbearable and Inman felt like something was wrong, so he called 911.

19 Sep 2019

Novel program that provides comprehensive care for Turner syndrome earns national recognition

A novel program designed to provide comprehensive care for Turner syndrome at The University of Texas Health Science Center at Houston and UT Physicians is one of the first in the U.S. to be designated an adult clinic by the Turner Syndrome Global Alliance.

24 May 2019

Ferring announces FDA approval of ZOMACTON for injection in four new pediatric indications

Ferring Pharmaceuticals Inc. today announced that the U.S. Food and Drug Administration has approved ZOMACTON for injection in four additional pediatric indications

20 Jul 2018

NIH researchers unravel how male, female mouse embryos acquire sex-specific reproductive systems

A protein called COUP-TFII determines whether a mouse embryo develops a male reproductive tract, according to researchers at the National Institutes of Health and their colleagues at Baylor College of Medicine, Houston.

17 Aug 2017

HSS researchers identify new way to quickly diagnose and treat Parsonage-Turner Syndrome

Physicians at Hospital for Special Surgery have been studying patient outcomes of Parsonage-Turner Syndrome (PTS), an uncommon neurological disorder that results in a sudden paralysis of one or more muscles around the shoulder and arm.

18 Oct 2016

Research: X and Y DNA swapping may occur more often than previously thought

It turns out that the rigid "line in the sand" over which the human sex chromosomes---the Y and X--- go to avoid crossing over is a bit blurrier than previously thought. Contrary to the current scientific consensus, Arizona State University assistant professor Melissa Wilson Sayres has led a research team that has shown that X and Y DNA swapping may occur much more often.

24 Mar 2016

Sex differences in the brain may provide clues to why certain forms of autism more common in males

Many early-onset neurodevelopmental disorders, including autism spectrum disorders, are more common in males than females. The origin of this gender bias is not understood, partially due to a major gap in research on sex differences regarding how the brain typically develops.

11 Dec 2015

Panorama SNP-based non-invasive prenatal test can detect complete molar pregnancy

Natera, Inc., a leader in non-invasive genetic testing, today announced a study published in Ultrasound in Obstetrics & Gynecology demonstrating that the Panorama single-nucleotide polymorphism (SNP)-based non-invasive prenatal test (NIPT) can identify a complete molar pregnancy in the first trimester.

From Natera 28 May 2015

First-of-its-kind DNA bank aims at advancing research into genetics of stuttering

Scientists at the University of Alberta's Institute for Stuttering Treatment and Research want Albertans to give a spit -- five millilitres to be precise -- to help find the cause and a cure for stuttering.

21 May 2015

Natera, LifeLabs sign new agreement for non-invasive prenatal testing in Canada

Natera, Inc., a global leader in non-invasive genetic testing, and LifeLabs Medical Laboratory Services today announced a new agreement that gives LifeLabs the rights to perform non-invasive prenatal testing (NIPT) in Canada using Natera technology.

From Natera 25 Apr 2015

Growth disorders in children can be detected earlier using new growth monitoring tools

Children's growth disorders can be detected earlier and more efficiently with the help of new growth monitoring tools, according to research from the University of Eastern Finland. These tools include up-to-date growth reference curves, evidence-based screening cut-off values for abnormal growth and automated growth monitoring based on electronic health records.

19 Mar 2015

Turner Syndrome News and Research

Further Reading

Genetic screening results just got harder to handle under new abortion rules

New mobile phone app could enable early identification of treatable growth disorders

Researchers report rare case of cardiac arrhythmias in a neonate with Turner syndrome

Microsurgery improves outcomes in patients experiencing paralysis from Parsonage-Turner Syndrome

HSS researchers use novel MRI technique to study Parsonage-Turner Syndrome

MGH researchers identify key mechanism in X chromosome inactivation

Cardiovascular surgeons heal a patient’s aortic dissection

Novel program that provides comprehensive care for Turner syndrome earns national recognition

Ferring announces FDA approval of ZOMACTON for injection in four new pediatric indications

NIH researchers unravel how male, female mouse embryos acquire sex-specific reproductive systems

HSS researchers identify new way to quickly diagnose and treat Parsonage-Turner Syndrome

Research: X and Y DNA swapping may occur more often than previously thought

Sex differences in the brain may provide clues to why certain forms of autism more common in males

Panorama SNP-based non-invasive prenatal test can detect complete molar pregnancy

First-of-its-kind DNA bank aims at advancing research into genetics of stuttering

Natera, LifeLabs sign new agreement for non-invasive prenatal testing in Canada

Growth disorders in children can be detected earlier using new growth monitoring tools

Scientists develop potential new therapy based on cow's immune molecules for hormone deficiencies

New toolkits help young adults navigate shift from pediatric to adult health care

Childhood oestrogen may normalise thelarche in Turner syndrome

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