301-310 of 1812 Results Found
Condition
Hereditary Hemochromatosis What is hereditary hemochromatosis? Hereditary hemochromatosis is a genetic blood disorder that causes your body to absorb too much iron from the food you eat. Iron is a mineral found in many foods. But too much iron is toxic to your body. The excess
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
Article
Parent management training: Making it work for your family
… inconsistency at home and a yo-yo effect on the moods of both parents and kids. Now, we’re not suggesting you try to … clean.” *Ding ding* an argument ensues! Sound familiar? As best as possible, you want to avoid words like “stop,” … the same household, divorced/separated parents, or even a grandparent who helps a lot. This inconsistency makes the …
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
Curricula & Schedules
The Pediatric Rheumatology Fellowship Training Program at Phoenix Children's is a comprehensive 36-month ACGME-accredited program focused on providing fellows with the necessary skills and knowledge to offer optimal care for pediatric patients with rheumatic diseases. The program
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
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