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Langerhans Cell Histiocytosis in Children What is Langerhans cell histiocytosis in children? Langerhans cell histiocytosis (LCH) is a rare disorder. It occurs when there are very high levels of a type of immune cell called a Langerhans cell. In the past, this disorder was thought

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

What Are Red Blood Cells? Red blood cells carry fresh oxygen all over the body. This is important to your health. Red blood cells are round with a flattish, indented center, like doughnuts without a hole. Your healthcare provider can check on the size, shape, and health of your

Blood Clotting Disorders in Children What are blood-clotting disorders in children? Blood-clotting disorders are a group of conditions in which there is too much clotting. Blood clotting is a normal process. It stops you from bleeding too much when you have a cut or injury. Blood

Dyskeratosis Congenita in Children What is dyskeratosis congenita in children? Dyskeratosis congenita is a congenital disease. This means it's present at birth. It's a very rare condition. It affects the skin and nails. In its most severe form, it causes bone marrow failure. When

Open Neural Tube Defects (ONTDs) in Children What are open neural tube defects in children? Open neural tube defects (ONTDs) are problems with the way the brain, spinal cord, or spine forms while a baby is growing in the pregnant person’s uterus. These problems occur in about 1

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 reaches from the

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

Emery-Dreifuss Muscular Dystrophy in Children What is Emery-Dreifuss muscular dystrophy in children? Emery-Dreifuss muscular dystrophy (EDMD) is one of the muscular dystrophies. These are a group of rare, inherited muscle diseases (myopathies). EDMD causes weakness in your child

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