From the beginning of care, through treatment, and into recovery, we provide an experience that’s right for children and families. Children’s National Health System provides a wide range of clinical services and specialties dedicated to improving children’s health.
Celiac disease is a genetic, autoimmune digestive disease that damages the small intestine and interferes with the absorption of nutrients from food.
Diseases of the kidneys often produce temporary or permanent changes to the small functional structures and vessels inside the kidney.
Osteogenesis imperfecta, also known as brittle-bone disease, is a genetic (inherited) disorder characterized by bones that break easily without a specific cause.
The term eating disorders refers to a variety of conditions that involve abnormal eating behaviors. Eating disorders are serious mental health problems that can be life-threatening, so they require clinical care by a physician or other healthcare professional.
Systemic lupus erythematosus, also known as SLE, or simply lupus, is a disease that is characterized by periodic episodes of inflammation of and damage to the joints, tendons, other connective tissues, and organs.
Muscular dystrophy describes a genetic disorder of the muscles that causes the muscles in the body to become very weak.
A seizure occurs when part(s) of the brain receives a burst of abnormal electrical signals that temporarily interrupts normal electrical brain function.
Sickle cell disease is an inherited blood disorder characterized by defective hemoglobin (a protein in red blood cells that carries oxygen to the tissues of the body).