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New guidelines recommend newborns with Down’s syndrome to receive leukemia test

New genetic testing has been developed at the University of Oxford to detect early signs of a potentially fatal condition that can also develop into full blown leukaemia in children with Down’s syndrome.

21 Jun 2018

Rhesus macaque model could be useful to test therapies for congenital Zika virus syndrome

Rhesus macaque monkeys infected in utero with Zika virus develop similar brain pathology to human infants, according to a report by researchers at the California National Primate Research Center and School of Veterinary Medicine at the University of California, Davis, published June 20 in Nature Communications.

21 Jun 2018

Scientists explore interactions between chromosomes 12 and 17

How are chromosomes arranged in the cell nucleus? Is it possible that they communicate with one another by "touching" each other?

21 Jun 2018

Combining stem cell technology and artificial intelligence to diagnose genetic cardiac diseases

A new study by Professors Martti Juhola and Katriina Aalto-Setälä of the University of Tampere in Finland demonstrates that with the use of artificial intelligence and machine learning, it is possible not only to accurately sort sick cardiac cell cultures from healthy ones, but also to differentiate between genetic cardiac diseases.

20 Jun 2018

Loyola Medicine study: Floppy eyelids linked to sleep apnea

A Loyola Medicine study is providing further evidence that floppy eyelids may be a sign of sleep apnea.

19 Jun 2018

Persistent psychological stress contributes to development and progression of vision loss

Persistent psychological stress, which is widely recognized as a consequence of vision loss, is also a major contributor to its development and progression, according to a study now published in the EPMA Journal, the official journal of the European Association for Predictive, Preventive, and Personalized Medicine.

19 Jun 2018

Inhibiting epigenetic proteins with drugs could prevent development of breast cancer

Researchers at the Princess Margaret Cancer Centre in Toronto have discovered that epigenetic proteins promote the proliferation of mammary gland stem cells in response to the sex hormone progesterone.

19 Jun 2018

Osteochondral knee defect treated using cell technology

As the publication describes, autologous cells of stromal vascular fraction were transplanted to a 36-year-old man with the use of fibrin matrix. The patient, whose injury had been caused by a fall, then has been under supervision for 2 years.

18 Jun 2018

Research explores role of autopsy in cardiovascular medicine

Autopsy is often an overlooked source of medical insight which may be hindering advances in cardiovascular medicine, according to new research published in a special issue of the American Heart Association's journal Circulation.

18 Jun 2018

New stimulation method increases hope for improving disorders of consciousness

To diagnose patients with severe brain injuries reliably, their state of consciousness has to be evaluated several times with suitable tools.

18 Jun 2018

New study focuses on best, cost effective practices to bridge treatment gap for brain disorders

Up to eight out of ten patients with a brain disorder remain untreated or inadequately treated. But what is the best practice - and above all, most cost effective - healthcare interventions to bridge the treatment gap? This was the focus of the European Brain Council's study entitled The Value of Treatment which was discussed at the Congress of the European Academy of Neurology in Lisbon.

18 Jun 2018

Sleep disorders appear to be first sign of serious neurological diseases

Sleep disorders are often the first sign of serious neurological diseases. Neurologists should inquire extensively about the quality of their patients' sleep.

18 Jun 2018

Technology breakthrough could enable detection of fetal genetic abnormalities in early pregnancy

A wide range of fetal genetic abnormalities could soon be detected in early pregnancy thanks to a world-first study led by University of South Australia researchers using lab-on-a-chip, non-invasive technology.

18 Jun 2018

Study suggests state-of-the-art genomic testing for routine autopsy of stillbirths

Pregnancy loss and the death of a newborn baby are devastating events, and as of today around 25% of these perinatal deaths are unexplained despite autopsy.

18 Jun 2018

Study provides insights into genetics underlying debilitating pediatric kidney disease

New research provides insights into the genetics underlying a debilitating kidney disease in children. The findings, which appear in an upcoming issue of the Journal of the American Society of Nephrology, could lead to new diagnostics and, ultimately, treatments.

14 Jun 2018

Abnormal sleep duration linked to metabolic syndrome in new study

Sleeping too little or even too much has been associated with several disease conditions including metabolic syndrome that predisposes a person to develop diabetes, stroke and heart disease. The findings of the study titled, “Association between sleep duration and metabolic syndrome: a cross-sectional study,” was published in the latest issue of the journal BMC Public Health.

14 Jun 2018

Syndrome News and Research

New guidelines recommend newborns with Down’s syndrome to receive leukemia test

Rhesus macaque model could be useful to test therapies for congenital Zika virus syndrome

Scientists explore interactions between chromosomes 12 and 17

Combining stem cell technology and artificial intelligence to diagnose genetic cardiac diseases

Loyola Medicine study: Floppy eyelids linked to sleep apnea

Persistent psychological stress contributes to development and progression of vision loss

Inhibiting epigenetic proteins with drugs could prevent development of breast cancer

Osteochondral knee defect treated using cell technology

Research explores role of autopsy in cardiovascular medicine

New stimulation method increases hope for improving disorders of consciousness

New study focuses on best, cost effective practices to bridge treatment gap for brain disorders

Sleep disorders appear to be first sign of serious neurological diseases

Technology breakthrough could enable detection of fetal genetic abnormalities in early pregnancy

Study suggests state-of-the-art genomic testing for routine autopsy of stillbirths

Study provides insights into genetics underlying debilitating pediatric kidney disease

Abnormal sleep duration linked to metabolic syndrome in new study

MSU scientists discover early cause of intestinal inflammation

Genetically engineered bacteria shows promise as new treatment for constipation

Etiologies of growing pains

Study unravels how nuclear pore complexes transport mRNAs out of the nucleus

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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