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Scientists use brain organoids to identify root causes of Miller-Dieker syndrome

Research led by scientists at UC San Francisco and Case Western Reserve University School of Medicine has used brain "organoids" — tiny 3D models of human organs that scientists grow in a dish to study disease — to identify root causes of Miller-Dieker Syndrome (MDS), a rare genetic disorder that causes fatal brain malformations.

7 Feb 2017

Penn scientists discover clues that could lead novel therapies for preventing heart failure

Of the more than 700,000 Americans who suffer a heart attack each year, about a quarter go on to develop heart failure.

7 Feb 2017

Study could provide novel therapeutic approach for preventing severe jaundice in newborn babies

For many newborn babies, an enzyme that breaks down the molecule bilirubin doesn't activate right away. The resulting bilirubin buildup can lead to jaundice, a typically harmless condition that causes a baby's skin to temporarily appear yellow.

6 Feb 2017

Maternal stress can affect growth of fetal muscles, study shows

Born too soon, she weighed just over 1 pound at birth and spent the first three months of her life in the neonatal intensive care unit, fighting to live.

6 Feb 2017

FDA grants permission to market new Seeker System for screening rare metabolic disorders in newborns

The U.S. Food and Drug Administration today permitted marketing of the Seeker System for the screening of four, rare Lysosomal Storage Disorders (LSDs) in newborns.

3 Feb 2017

Thirdhand smoke exposure leads to biological effects on weight and cell development

The sticky residue left behind by tobacco smoke can do worse damage than stinking up furniture and discoloring walls.

3 Feb 2017

Experts update cystic fibrosis guidelines for better diagnosis and personalized treatment

An international research group of 32 experts from nine countries has updated the guidelines for diagnosing the genetic disease cystic fibrosis.

31 Jan 2017

Scientists decode genetic profile of rare inherited disorder that can cause genital ambiguity

A complete clinical and genetic profile of a rare inherited disorder, steroid 11-hydroxylase deficiency, which can cause genital masculinization in females, is being reported by an international group of researchers led by investigators at the Icahn School of Medicine at Mount Sinai.

30 Jan 2017

IQWiG assesses benefit of newborn screening for severe combined immunodeficiency

The German Institute for Quality and Efficiency in Health Care assessed the benefit of newborn screening for severe combined immunodeficiency (SCID).

30 Jan 2017

Orthopaedic research helps nurse recover from knee injury

Working as a bedside nurse requires extensive physical effort — pushing wheelchairs and beds, twisting and lifting, and long periods on your feet.

28 Jan 2017

Marginal deficiency of vitamin A in fetus or newborns may lead to Alzheimer's disease in later life

Biochemical reactions that cause Alzheimer's disease could begin in the womb or just after birth if the fetus or newborn does not get enough vitamin A, according to new research from the University of British Columbia.

27 Jan 2017

New gene therapy for Pompe disease may replace currently available treatments

After decades investigating a rare, life-threatening condition that cripples the muscles, Duke Health researchers have developed a gene therapy they hope could enhance or even replace the only FDA-approved treatment currently available to patients.

27 Jan 2017

Johns Hopkins researchers create mature cardiomyocytes in the laboratory from stem cells

Generating mature and viable heart muscle cells from human or other animal stem cells has proven difficult for biologists.

26 Jan 2017

Utah law increases early identification of infants with hearing loss, new study reveals

A Utah law has led to increased early identification of infants with hearing loss due to a congenital infection, according to a new study by University of Utah and Utah Department of Health researchers.

25 Jan 2017

Researchers find brain abnormalities in Zika virus infected fetuses

In a study to be presented Friday, Jan. 27, in the oral concurrent session at 1:15 p.m. PST, at the Society for Maternal-Fetal Medicine's annual meeting, The Pregnancy Meeting, researchers with the Baylor College of Medicine Department of Obstetrics and Gynecology, Houston, Texas partnered with the Maternal-Fetal Unit, CEDIFETAL, Centro de Diagnostico de Ultrasonido e Imagenes, CEDIUL, Barranquilla, Columbia and the Unidad De Fertildad Y Genetica De Cartagena, Cartagena de Indias, Columbia, to create the study, Characterization of brain malformations and volume assessment in fetuses with Zika Virus infection using MRI.

24 Jan 2017

Study looks at use of evolutionary triangulation to refine results from genetic studies of preterm birth

In a study to be presented Thursday, Jan. 26, in the oral concurrent session at 1:15 p.m. PST, at the Society for Maternal-Fetal Medicine's annual meeting, The Pregnancy Meeting, researchers verified genetic results from one large study of women with spontaneous preterm birth, and highlighted 13 key genes in both mothers and babies which may be involved in preterm birth while also identifying 123 genes as top candidates for further study.

23 Jan 2017

Newborn News and Research

Scientists use brain organoids to identify root causes of Miller-Dieker syndrome

Penn scientists discover clues that could lead novel therapies for preventing heart failure

Study could provide novel therapeutic approach for preventing severe jaundice in newborn babies

Maternal stress can affect growth of fetal muscles, study shows

FDA grants permission to market new Seeker System for screening rare metabolic disorders in newborns

Thirdhand smoke exposure leads to biological effects on weight and cell development

Experts update cystic fibrosis guidelines for better diagnosis and personalized treatment

Scientists decode genetic profile of rare inherited disorder that can cause genital ambiguity

IQWiG assesses benefit of newborn screening for severe combined immunodeficiency

Orthopaedic research helps nurse recover from knee injury

Marginal deficiency of vitamin A in fetus or newborns may lead to Alzheimer's disease in later life

New gene therapy for Pompe disease may replace currently available treatments

Johns Hopkins researchers create mature cardiomyocytes in the laboratory from stem cells

Utah law increases early identification of infants with hearing loss, new study reveals

Researchers find brain abnormalities in Zika virus infected fetuses

Study looks at use of evolutionary triangulation to refine results from genetic studies of preterm birth

Study finds great variations in view of withdrawing futile treatment for terminally ill patients

Number of U.S. women taking maternity leave has not changed, study finds

Researchers explore ins and outs of genome sequencing in newborns

Researchers show how adult learning is impaired in females using mouse models of Rett syndrome

Evaluating new approaches for rare disease genomics

Expanding access to NMR with the Fourier 80 Duo

Advancing Intracellular Delivery with LumiPore®

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