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Children's National Hospital


Children's National collaborates with NIH researchers to identify gene variant in Proteus syndrome

A team of researchers at Children's National Medical Center has identified the genetic mutation causing Proteus syndrome, a rare disorder characterized by excessive tissue and bone growth. The study found that a point mutation in the AKT1 gene activates sporadic tissue growth associated with Proteus syndrome.

SourceChildren's National Hospital·JournalNew England Journal of Medicine·DateAug 10, 2011

Study: Lap band surgery effective for morbidly obese children

A new study published in the Journal of the American College of Surgeons found that laparoscopic adjustable gastric banding (Lap band) surgery improves the health of morbidly obese adolescents. The procedure led to significant weight loss and reduced the risk of developing insulin resistance, a key indicator of obesity-related illnesses.

SourceChildren's National Hospital·JournalJournal of the American College of Surgeons·DateNov 3, 2009

First treatment for muscular dystrophy in sight: Scientists successfully harness exon-skipping

Researchers at Children's National Medical Center and colleagues in Tokyo have achieved the first successful application of exon-skipping to curb Duchenne muscular dystrophy in dogs. The treatment uses synthetic DNA-like molecules called morpholinos to skip over mutated gene parts, showing promise for humans with this genetic disorder.

SourceChildren's National Hospital·JournalAnnals of Neurology·DateMar 16, 2009

Children's National research links platelets to sepsis-related organ failure

Scientists have identified platelets as a contributor to organ failure in patients with sepsis. The study found that granzyme B production in platelets can cause cell death, leading to organ failure. Researchers hope this discovery will lead to better treatments and potentially even prevention of organ failure.

SourceChildren's National Hospital·JournalAmerican Journal of Respiratory and Critical Care Medicine·DateMar 10, 2009