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Diamond Blackfan Anemia (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. Learn about symptoms, diagnosis, and treatment of DBA.
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PFAPA Syndrome
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.
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Duchenne Muscular Dystrophy in Children
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.
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Emery-Dreifuss Muscular Dystrophy in Children
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.
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Facioscapulohumeral Muscular Dystrophy in Children
FSHD is a rare genetic muscle disease that affects the muscles of your child’s face, shoulders, upper arms, and lower legs.
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Astrocytoma in Children
Astrocytoma is the most common type of brain tumor in children. It is usually low grade, which means slow-growing.
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Oligodendroglioma in Children
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.
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Achalasia in Children
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).
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Burners and Stingers Syndrome in Children
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.
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Showing 6814 - 6822 of 12682 results