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Diamond Blackfan Anemia (DBA) in Children What is DBA in children? Diamond Blackfan anemia (DBA) is a rare blood disorder. Children with DBA don't make enough red blood cells. These cells carry oxygen to all other cells in the body. Blood cells are made in the bone marrow, the

Tongue-Tie (Ankyloglossia) in Children What is tongue-tie in children? Tongue-tie (ankyloglossia) is a problem with the tongue that is present from birth. It causes speech and eating problems in some children. The lingual frenulum of the tongue is a small fold of tissue that

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

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

Neonatal Hypoxic-Ischemic Encephalopathy What is neonatal hypoxic-ischemic encephalopathy? Hypoxic-ischemic encephalopathy (HIE) is a type of brain damage. It’s caused by a lack of oxygen to the brain before or shortly after birth. It affects the central nervous system. Babies

MRSA Infection in Children What is MRSA in children? Staphylococcus aureus (staph) is a type of bacteria. Methicillin-resistant Staphylococcus aureus (MRSA) is a staph infection that has become resistant to many antibiotics commonly used to treat staph infections. MRSA is usually

Fanconi Anemia in Children What is Fanconi anemia in children? Fanconi anemia is a blood disorder. The bone marrow either doesn't make enough blood cells or it makes abnormal blood cells. Bone marrow is the spongy material inside bones. It makes white and red blood cells, and

Von Willebrand Disease (VWD) What is VWD? Von Willebrand disease (VWD) is an inherited disorder that affects the blood's ability to clot. What causes VWD? VWD is almost always inherited. This means it is passed from parents to children. People with the disorder may have low

Achalasia in Children What is achalasia in a child? Achalasia is a rare disease that makes it hard to swallow foods and liquids. In achalasia, there is a problem with the tube that carries food from the mouth to the stomach (esophagus). The muscles that make the esophagus