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Research links DNA variants to increased risk of IBS in women

New research coordinated by Karolinska Institutet in Sweden links certain DNA variants to increased risk of irritable bowel syndrome in women. The findings, published in the scientific journal Gastroenterology, might help explain why IBS is more common in women than in men.

5 Apr 2018

Study reveals differences in the brains of children with fragile X syndrome

For the first time, UNC School of Medicine researchers have used MRIs to show that babies with the neurodevelopmental condition fragile X syndrome had less-developed white matter compared to infants that did not develop the condition.

4 Apr 2018

Sulfur amino acid restriction consistently demonstrates range of health benefits in animals

The longevity and health improvements seen in animals on sulfur amino acid-restricted diets could translate to people, according to Penn State College of Medicine researchers who recently conducted a review of published studies. More research is needed to confirm the benefits in people, the scientists said.

4 Apr 2018

NYU Langone Health surgeons successfully perform first lung transplant procedure

Shortly after receiving final regulatory approval to launch a new lung transplant program, NYU Langone Health surgeons successfully performed the institution's first procedure, giving two new lungs - and a new lease on life - to a Brooklyn woman with a complicated form of pulmonary fibrosis.

2 Apr 2018

SIDS study reveals unsafe sleep practices among babysitters, relatives and friends

Babies who died during their sleep while being watched by someone other than parents often had been placed in unsafe sleep positions, such as on their stomachs, or in unsafe locations, such as a couch, a new study has found.

2 Apr 2018

FDA grants accelerated approval to leukemia drug for patients with MRD-positive ALL

The U.S. Food and Drug Administration granted accelerated approval to Blincyto (blinatumomab) to treat adults and children with B-cell precursor acute lymphoblastic leukemia (ALL) who are in remission but still have minimal residual disease (MRD).

30 Mar 2018

Alfred Blalock’s medical breakthroughs have been saving many lives

The year was 1925, and Alfred Blalock was already a failure at age 26. The born-and-raised Georgian earned a bachelor's degree from the University of Georgia in 1918, then a medical doctorate from Johns Hopkins University four years later. But he didn't get the surgical residency he coveted at Hopkins; he ended up interning in urology instead.

29 Mar 2018

New review explores potentially safer therapies for treating chronic abdominal pain

An estimated 2 million people in the U.S. are addicted to prescription opioids- powerful doctor-prescribed medications for chronic or severe pain. The drugs are commonly prescribed to treat gastrointestinal pain caused by conditions such as Crohn's disease and irritable bowel syndrome (IBS), raising the risk of addiction among this population.

29 Mar 2018

Genomic test effective for detecting Lynch syndrome in CRC patients

A single, upfront genomic test is more effective for detecting Lynch syndrome in colorectal cancer (CRC) patients than the traditional multiple, sequential testing approach, according to new clinical data reported by The Ohio State University Comprehensive Cancer Center - Arthur G. James Cancer Hospital and Richard J. Solove Research Institute.

29 Mar 2018

Study identifies potential genetic link in sudden infant death syndrome

Rare genetic mutations associated with impairment of the breathing muscles are more common in children who have died from sudden infant death syndrome (also known as ‘cot death’) than in healthy controls, suggesting a possible genetic element of the disorder, according to a case-control study in the UK and USA published in The Lancet.

29 Mar 2018

Genetic links to cot deaths found in new research

Cot death or Sudden Infant Death Syndrome (SIDS) is a rare but unexplained and tragic occurrence where babies between ages two and four months who are apparently healthy die unexpectedly during sleep. SIDS is responsible for around 300 and 2400 deaths in the United Kingdom and United States of America yearly. Researchers have now found a genetic link that could explain the occurrence and risk of such incidents. The study appeared in the latest issues of the journal Lancet.

29 Mar 2018

Researchers highlight the need to reconsider mitochondrial replacement moratorium

Mothers with mitochondrial DNA mutations often give birth to children who face incurable and fatal illnesses. But a much-studied form of mitochondrial replacement could prevent the transmission of such diseases from mothers to children, researchers say.

28 Mar 2018

Researchers aim to reveal new direction for Barth syndrome treatment

The Barth Syndrome Foundation recently announced awardees from its 2017 grant cycle. Miriam Greenberg, Ph.D., professor of biological sciences in the College of Liberal Arts and Sciences at Wayne State University and a resident of Ann Arbor, Michigan, received a one-year, $50,000 grant for the project, "Cardiolipin activates pyruvate dehydrogenase (PDH) - a potential new target for treatment of Barth syndrome."

28 Mar 2018

Researchers probe RNA epigenetics and chromatin structures to predict drug resistance in leukemia

Drug resistance is a major obstacle to effective treatment for patients with cancer and leukemia. Epigenetic modifying drugs have been proven effective for some patients with hematologic malignancies, such as myelodysplastic syndrome (MDS) and acute myeloid leukemia (AML).

23 Mar 2018

Genetic mutation that may protect people from malaria found to be more common

A genetic mutation that may protect people from malaria, but was thought to be rare, is surprisingly common, suggest the findings of a new study led by scientists at The Scripps Research Institute.

23 Mar 2018

Researchers uncover cause of rare childhood neurodegenerative disease

Neurology researchers investigating a rare but devastating neurological regression in infants have discovered the cause: gene mutations that severely disrupt crucial functions in mitochondria, the energy-producing structures within cells.

23 Mar 2018

Maternal obesity and androgen excess induce sex-specific anxiety in offspring, study suggests

Maternal obesity and androgen excess induce sex-specific anxiety in the offspring, according to a study on mice by researchers at Karolinska Institutet in Sweden published in The FASEB Journal.

22 Mar 2018

Vitamin D deficiency linked to metabolic syndrome in postmenopausal women

Results of a study carried out in Brazil showed a strong association between vitamin D deficiency and metabolic syndrome in postmenopausal women.

21 Mar 2018

Research shows link between chronic fatigue syndrome and lower thyroid hormone levels

New research demonstrates a link between chronic fatigue syndrome (CFS) symptoms and lower thyroid hormone levels. Published in Frontiers in Endocrinology, the study indicates that CFS, a condition with unknown causes, can be explained by lower thyroid hormones -- but may be distinct from thyroidal disease.

20 Mar 2018

Study: Premature babies have higher risks of health complications in Bangladesh

A recently published study in Bangladesh titled Clinical outcome of the late preterm infants shows that premature babies can develop major neonatal complications that need admission in a neonatal intensive care unit.

20 Mar 2018

Syndrome News and Research

Research links DNA variants to increased risk of IBS in women

Study reveals differences in the brains of children with fragile X syndrome

Sulfur amino acid restriction consistently demonstrates range of health benefits in animals

NYU Langone Health surgeons successfully perform first lung transplant procedure

SIDS study reveals unsafe sleep practices among babysitters, relatives and friends

FDA grants accelerated approval to leukemia drug for patients with MRD-positive ALL

Alfred Blalock’s medical breakthroughs have been saving many lives

New review explores potentially safer therapies for treating chronic abdominal pain

Genomic test effective for detecting Lynch syndrome in CRC patients

Study identifies potential genetic link in sudden infant death syndrome

Genetic links to cot deaths found in new research

Researchers highlight the need to reconsider mitochondrial replacement moratorium

Researchers aim to reveal new direction for Barth syndrome treatment

Researchers probe RNA epigenetics and chromatin structures to predict drug resistance in leukemia

Genetic mutation that may protect people from malaria found to be more common

Researchers uncover cause of rare childhood neurodegenerative disease

Maternal obesity and androgen excess induce sex-specific anxiety in offspring, study suggests

Vitamin D deficiency linked to metabolic syndrome in postmenopausal women

Research shows link between chronic fatigue syndrome and lower thyroid hormone levels

Study: Premature babies have higher risks of health complications in Bangladesh

Bringing real-time analytics to downstream bioprocess monitoring

Designing fluidic architecture for scalable diagnostic platforms

Evaluating new approaches for rare disease genomics

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