251-260 of 1488 Results Found
Social Media Guidelines: Engagement on Phoenix Children’s Public Platforms
Social media is for everyone. It enables us to interact with our patients, families, donors and anyone else who is passionate about Phoenix Children’s, the work we do and our immediate community. We encourage you to be active participants in our online communities. These are the
Condition
Facioscapulohumeral Muscular Dystrophy in Children What is FSHD in children? Facioscapulohumeral muscular dystrophy (FSHD) is a rare genetic muscle disease that affects the muscles of your child’s face, shoulders, upper arms, and lower legs. These muscles weaken and shrink
Doctor
Joshua D. Koch, MD
Co-Director, Center for Heart Care; Division Chief, Cardiac Critical Care Medicine; Division Chief, Pediatric Critical Care Medicine
Specialties
Condition
Nosebleed (Epistaxis) in Children What is a nosebleed in children? A nosebleed is bleeding from tissues inside the nose (nasal mucus membranes) caused by a broken blood vessel. The medical word for nosebleed is epistaxis. Most nosebleeds in children occur in the front (anterior)
Condition
Tracheoesophageal Fistula and Esophageal Atresia What are tracheoesophageal fistula and esophageal atresia? Tracheoesophageal fistula Tracheoesophageal fistula is a connection between the esophagus and the trachea. The esophagus is the tube that connects the throat to the stomach
Condition
Voice Disorders What are voice disorders? You may have a voice disorder if you have a problem with pitch, volume, tone, and other qualities of your voice. These problems occur when your vocal cords don't move or vibrate normally. Your voice is the sound that air makes when it is
Condition
Color Blindness What is color blindness? Color blindness is when you see colors differently than most people do. The retina is the light-sensitive lining in the back part of your eye. It sends visual information to your brain. Your retina has special cells that detect color
Condition
Osteogenesis Imperfecta in Children What is osteogenesis imperfecta in children? Osteogenesis imperfecta (OI) is a rare inherited (genetic) bone disorder that is present at birth. It's also known as brittle bone disease. A child born with OI may have soft bones that break