HHT conference adds children-focused programming, study enrollment
The Hereditary Hemorrhagic Telangiectasia (HHT) Foundation’s 15th Annual Patient and Family conference will be held Oct. 22-24 at the Eric P. Newman Education Center. The event will bring together specialists to provide education and support for adult and pediatric patients with HHT and their families.
Newborns with respiratory distress potentially have rare genetic disease
Newborns with respiratory distress should be evaluated for primary ciliary dyskinesia, a rare genetic disease that has features similar to cystic fibrosis, says Thomas Ferkol from the School of Medicine. He reports finding that about 80 percent of patients with primary ciliary dyskinesia (PCD) have a history of newborn respiratory distress.
Newborns with respiratory distress potentially have rare genetic disease
Newborns with respiratory distress should be evaluated for primary ciliary dyskinesia, a rare genetic disease that has features similar to cystic fibrosis, says Thomas Ferkol from Washington University School of Medicine in St. Louis. He reports finding that about 80 percent of patients with primary ciliary dyskinesia (PCD) have a history of newborn respiratory distress.