How a leukemia hijacks the genes needed by blood stem cells
As a child, Lynn Aureli didn’t know that a particular genetic change contributed to her acute myeloid leukemia (AML) — an alteration that eventually would help explain the cancer’s lack of response to chemotherapy. Nor was she aware that her cancer had hijacked the genetic mechanism for maintaining the stem cells that form blood, like ... Read More about How a leukemia hijacks the genes needed by blood stem cells
Research opens a window into understanding deadly brain tumors
Formerly known as diffuse intrinsic pontine gliomas, diffuse midline gliomas (DMGs) are highly aggressive tumors found in the midline of the brain. Their prognosis is very poor, in part because they don’t respond well to treatments such as chemotherapy and radiation. Now, research by Mariella Filbin, MD, PhD, and others in the Brain Tumor Center ... Read More about Research opens a window into understanding deadly brain tumors
Understanding BRUEs: Recent study sheds light
Brief resolved unexplained events (BRUEs) are episodes marked by concerning changes in breathing, consciousness, muscle tone, and skin color (cyanosis or paleness). They tend to occur in previously healthy infants and send worried parents racing to the emergency department. However, researchers know little about the risk of persistent symptoms after BRUE hospitalizations. To learn more, ... Read More about Understanding BRUEs: Recent study sheds light
AI could change the way we look at hip preservation
Orthopedic surgeons and biomedical engineers are trained to approach adolescent and young adult hip pain from two different perspectives. Surgeons typically look at conditions such as femoroacetabular impingement (FAI) and hip dysplasia from a clinical point of view. Engineers more often focus on the technology angle. These two perspectives have come together at Boston Children’s ... Read More about AI could change the way we look at hip preservation
I-PASS this patient to you: Improved hospital ‘handoffs’ cut adverse events by almost half
About 15 years ago, Boston Children’s Hospital pediatricians Christopher Landrigan, MD, MPH, and Amy Starmer, MD, MPH, observed a weak link in hospital care. Medical residents were rigorously trained to take patient histories with standardized templates and to present cases in a structured format during daily rounds. Yet such structured communication was largely absent at ... Read More about I-PASS this patient to you: Improved hospital ‘handoffs’ cut adverse events by almost half
‘On fire’ with sJIA: When arthritis is much more than joint pain
Georgia is finally living her best life. Her toddler years were challenging: At 15 months old, a series of high fevers landed her at Boston Children’s Hospital for two weeks. After many rounds of tests looking for infection and a bone marrow biopsy to rule out cancer, she was diagnosed with systemic juvenile idiopathic arthritis ... Read More about ‘On fire’ with sJIA: When arthritis is much more than joint pain
Obesity is increasing people’s risk of cancer. Why?
Obesity is now a global epidemic, and it is increasing people’s risk for cancer. The National Cancer Institute lists more than a dozen cancers that are associated with overweight and obesity. But how obesity increases cancer risk hasn’t been clear. The lab of Marsha A. Moses, PhD, at Boston Children’s Hospital, now draws a direct ... Read More about Obesity is increasing people’s risk of cancer. Why?
Predicting feeding difficulties in children with esophageal atresia: A proactive approach
Children with esophageal atresia are at risk for developing anastomotic strictures, or areas of esophageal narrowing, following surgical repair. Clinicians have long assumed that such strictures can cause dysphagia and feeding difficulties, but it isn’t clear whether the severity of feeding difficulties is related to the severity of a stricture. Now, findings of a recent ... Read More about Predicting feeding difficulties in children with esophageal atresia: A proactive approach
Chromosomal testing expands options for exploring causes of SIDS
When an infant or young child dies without explanation, it is not uncommon for parents to blame themselves. In some cases, unfortunately, they may be wrongly investigated by the authorities, even as they yearn for answers themselves. Most often, these answers never come. But research is slowly starting to change that. Increasing evidence suggests that ... Read More about Chromosomal testing expands options for exploring causes of SIDS
Genetic sequencing may open doors for newborns with hypotonia
When a baby is born with low muscle tone (hypotonia), the future is hard to predict, and families have a lot of questions. How should neonatologists care for these infants? Findings from a recent review could help provide some answers, guide appropriate interventions, and in some cases open the way to custom treatments. Diagnosing a ... Read More about Genetic sequencing may open doors for newborns with hypotonia