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A mother and daughter consulting with a doctor, as occurs in the Children's Rare Disease Collaborative.

Changing lives through genetics: The Children’s Rare Disease Collaborative

Clinical Care, Research
A 14-year-old girl was having back pain after a car accident and visited an orthopedic clinic at Boston Children’s Hospital. In the course of her care, she joined the Children’s Rare Disease Collaborative (CRDC), a hospital-wide effort to enroll children and adults with rare diseases in genetic studies. Genetic testing revealed that both she and ... Read More about Changing lives through genetics: The Children’s Rare Disease Collaborative
Tagged: diagnostics, genetics and genomics, rare disease, research
Multiple pipettes filling a 96-well plate.

Model enables study of age-specific responses to COVID mRNA vaccines in a dish

Clinical, Research
mRNA vaccines clearly saved lives during the COVID-19 pandemic, but several studies suggest that older people had a somewhat reduced immune response to the vaccines when compared with younger adults. Why? Researchers at Boston Children’s Hospital, led by Byron Brook, PhD, David Dowling, PhD, and Ofer Levy, MD, PhD, found some answers — while providing ... Read More about Model enables study of age-specific responses to COVID mRNA vaccines in a dish
Tagged: coronavirus, immunology, infectious diseases, vaccines
The crystal structure of 4 connected BCL11A proteins, the basis for a possible sickle cell drug.

Could a pill treat sickle cell disease?

Basic/Translational, Research
The new gene therapies for sickle cell disease — including the gene-editing treatment Casgevy, based on research at Boston Children’s Hospital — have been game-changing for the patients who have received them. But Stuart Orkin, MD, the Boston Children’s hematologist whose work led the way to Casgevy, wants to go even further. “The editing therapy ... Read More about Could a pill treat sickle cell disease?
Tagged: drug development, hematology, sickle cell disease
A smiling Branden Baptiste in front of the Boston Children’s Hospital entrance, after his base editing treatment.

A sickle cell first: Base editing, a new form of gene therapy, leaves Branden feeling ‘more than fine’

Clinical, Research
Though he doesn’t remember it, Branden Baptiste had his first sickle cell crisis at age 2. Through elementary school, he was in and out of the hospital with pain episodes, not knowing why. As he got older, he learned he had sickle cell disease. His red blood cells were forming sickle shapes and getting stuck ... Read More about A sickle cell first: Base editing, a new form of gene therapy, leaves Branden feeling ‘more than fine’
Tagged: clinical trials, gene editing, gene therapy, hematology, sickle cell disease
A big syringe, held by a researcher, contains gas microbubbles that aim to deliver emergency oxygen.

Injected microbubbles could be a safe way to deliver emergency oxygen

Basic/Translational, Research
For years, researchers and clinicians have been trying to find a way to rapidly deliver oxygen to patients when traditional means of oxygenation are difficult or ineffective during critical moments of cardiac or respiratory arrest. Sometimes, hypoxemia caused by airway obstruction or lung disease can be so severe that methods to boost low-oxygen levels (including ... Read More about Injected microbubbles could be a safe way to deliver emergency oxygen
Tagged: cardiac research, cardiology, drug development, emergency medicine, heart, heart center, research
A strip of DNA spawning red blood cells, conveying the idea of gene therapy for Diamond Blackfan anemia.

A universal gene therapy for Diamond-Blackfan anemia is poised for clinical testing

Basic/Translational, Research
Diamond-Blackfan anemia (DBA), first described at Boston Children’s Hospital in 1938, is a rare blood disorder in which the bone marrow cannot make mature, functioning red blood cells. Children with this life-threatening anemia have few treatment options. A small handful with a well-matched donor can be cured with bone marrow transplant, but most rely on ... Read More about A universal gene therapy for Diamond-Blackfan anemia is poised for clinical testing
Tagged: anemia, blood, blood disorder, gene therapy, hematology
A spherical skin organoid showing blood vessels intermingled with hair.

Skin organoid could guide new treatments for skin conditions, hair loss

Basic/Translational, Research
What does it take to build healthy skin? Two research groups converged on this question from different angles. They’ve now produced the most detailed view to date of the cell types and cell collaborations that go into creating our body’s largest organ. Several years ago, Karl Koehler, PhD, and colleagues at Boston Children’s Hospital used ... Read More about Skin organoid could guide new treatments for skin conditions, hair loss
Tagged: organoids, plastic surgery
Runners competing in the Boston Marathon.

Fuel to be faster: Studying the effects of low energy availability at the Boston Marathon

Clinical, Research
Like many sports medicine specialists, Kristin Whitney, MD, MA, suspected that many of the issues she treats in runners — bone stress injuries, anemia, decreased response to training, and reduced endurance to name a few — stemmed from insufficient nutrition. Key takeaways Runners with indicators of low energy availability had slower finish times and more ... Read More about Fuel to be faster: Studying the effects of low energy availability at the Boston Marathon
Tagged: orthopedics, running injury, sports injury, sports medicine
Professionals of diverse races join hands.

Making pediatric health equity research truly equitable: An EDI review process

Clinical, Research
A burgeoning number of studies are examining pediatric health equity, diversity, and inclusion (EDI). But if not done right, health equity research can do a disservice, perpetuating biases and wrong assumptions that actually exacerbate inequities. To guide EDI-related studies, the Institutional Review Board (IRB) at Boston Children’s Hospital (through Tina Young Poussaint, MD, and Susan ... Read More about Making pediatric health equity research truly equitable: An EDI review process
Tagged: health equity, research
A pregnant women holding her belly by a window.

Mutations during prenatal development may contribute to schizophrenia

Basic/Translational, Research
Schizophrenia is known to have a genetic component, and variants in 10 genes have been identified as markedly increasing schizophrenia risk. But together, these genes account for under 5 percent of cases. Now, a pilot study in the journal Science suggests another important contributor to schizophrenia: distinctive patterns of non-inherited (somatic) mutations. These mutations appear ... Read More about Mutations during prenatal development may contribute to schizophrenia
Tagged: genetics and genomics, neuroscience, schizophrenia

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