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PFAPA is a childhood syndrome that causes repeated episodes of fever, mouth sores, sore throat, and swollen lymph nodes. PFAPA usually starts in early childhood between ages 2 and 5.

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.

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.

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

Astrocytoma is the most common type of brain tumor in children. It is usually low grade, which means slow-growing.

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.

Achalasia is a rare disease that makes it hard to swallow food and liquids. In achalasia, there is a problem with the tube that carries food from the mouth to the stomach (esophagus).

Burners and stingers syndrome is a type of sports injury. It is a pain in the shoulder or neck that causes a burning or stinging feeling down an arm to the hand.

Hypothyroidism is when the thyroid gland doesn't make enough thyroid hormone. The condition is more common in adults. But it’s the most common thyroid disorder in children. Not enough thyroid hormone leads to signs, such as slow growth, lack of activity, and poor performance in school.