Burkitt lymphoma is a rare, fast-growing form of non-Hodgkin lymphoma (NHL). It’s a type of cancer of the lymphatic system. The lymphatic system is part of the immune system. It helps to fight diseases and infections.

Sports medicine healthcare providers have special training to restore function to injured patients so they can get moving again as soon as possible. They are experts on preventing illness and injury in active people.

The brain is part of the central nervous system (CNS). The CNS also includes the spinal cord. A tumor is an abnormal growth of tissue. An oligodendroglioma is a type of CNS tumor called a glioma.

FSHD is a rare genetic muscle disease that affects the muscles of your child’s face, shoulders, upper arms, and lower legs.

Pulmonary interstitial emphysema (PIE) is when air gets trapped in the tissue outside the tubes and air sacs of the lungs. It affects newborn babies. PIE is fairly common in neonatal intensive care units (NICUs).

A nasal fracture is a break in one or more of the bones of the nose, caused by trauma. It's also called a broken nose.

Childhood apraxia of speech is a type of speech disorder. It is present from birth. A child with this condition has problems making sounds correctly and consistently.

Aplastic anemia is a rare blood disorder that most often occurs in children, teens, and young adults. This piece offers helpful information on how to help your child live with this disease.

EDMD is a rare inherited muscle disease. It causes weakness in your child’s shoulders, upper arms, and calves. The disease also causes stiff joints that can’t move well.

Duchenne muscular dystrophy is a rare genetic condition that weakens your child's muscles. It appears in young boys, usually between ages 2 and 5.