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Beta Thalassemia in Children What is beta thalassemia in children? Beta thalassemia is an inherited blood disorder. This means it's passed down through a parent’s genes. It's a form of anemia. Anemia is a low red blood cell or low hemoglobin level. Hemoglobin is part of red blood

Polio (Poliomyelitis) What is polio? Poliomyelitis is commonly called polio. It's an infectious disease. It is caused by 1 of 3 types of poliovirus. Polio is easily spread from person to person. The poliovirus is a virus that can cause paralysis. But most people who are infected

Guillain-Barré Syndrome in Children What is Guillain-Barré syndrome in children? Guillain-Barré syndrome (GBS) is a short-term but often life-threatening disorder that affects the nerves in the body. GBS can cause muscle weakness, pain, and short-term (temporary) paralysis of the

Necrotizing Enterocolitis in the Newborn What is necrotizing enterocolitis in the newborn? Necrotizing enterocolitis (NEC) is a serious, life-threatening illness in newborns. It happens when tissue in the large intestine (colon) gets inflamed. This inflammation damages and kills

Chronic Liver Disease/Cirrhosis What is cirrhosis? Cirrhosis is when scar tissue replaces healthy liver tissue. This stops the liver from working normally. Cirrhosis is a long-term (chronic) liver disease. The damage to your liver builds up over time. The liver is your body’s

Claudication What is claudication? Claudication is pain in your thigh, calf, or buttocks that happens when you walk. It can make you limp. It may be a symptom of peripheral artery disease (PAD). This is when narrowed or blocked arteries reduce the blood flow to your legs. At

Appendicitis What is appendicitis? Appendicitis is a medical emergency. It happens when your appendix becomes sore, swollen, and diseased. The appendix is a thin tube that is joined to the large intestine. It sits in the lower right part of your belly (abdomen). The appendix is a

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

Duchenne Muscular Dystrophy in Children What is Duchenne muscular dystrophy in children? Duchenne muscular dystrophy (DMD) is a genetic condition that weakens your child’s muscles. It is the most common muscular dystrophy, a kind of inherited muscle disease. DMD causes weakness

Achondroplasia in Children What is achondroplasia in a child? Achondroplasia is the most common type of rare genetic bone disorder. The strong, flexible tissue called cartilage is not made into bone as normal. This causes a series of signs, such as short arms and legs and a large