131-140 of 340 Results Found
Condition
Cataracts in Children What are cataracts in children? A cataract is a clouding of the eye's lens. The lens is normally clear (transparent). Cataracts keep light rays from passing through the lens and focusing on the retina. The retina is the thin layer of nerve tissue that lines
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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
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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
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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
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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)
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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
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Maternal and Fetal Testing Overview Most people have healthy pregnancies, and their babies are born without trouble. But people with high-risk pregnancies often need to be closely watched for possible problems. Fortunately, many tests and procedures are available to keep track of
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Trisomy 13 and Trisomy 18 in Children What are trisomy 13 and trisomy 18 in children? Trisomy 13 and trisomy 18 are genetic disorders. They include a combination of birth defects. This includes severe learning problems and health problems that affect nearly every organ in the
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Uniparental Disomy: Prader-Willi Syndrome and Angelman Syndrome What is uniparental disomy? Chromosome pairs affect how our body works. Normally, a baby gets 1 copy of each chromosome pair from each parent. This means 1 copy from the genetic mother, and the other copy from the
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Occupational Lung Diseases What are work-related lung diseases? Work-related lung diseases are lung problems that are caused by certain work environments. They are caused by breathing materials into the lungs. These lung diseases may have lasting effects, even after the exposure