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Secondary Carnitine Deficiency
Carnitine is a nutrient that helps the body's cells work normally. Secondary carnitine deficiency is when there isn't enough carnitine in the blood. Read this to learn more about this condition, including the causes, symptoms, ways to diagnose it, and the treatment options.
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Neuronal and Mixed Neuronal-Glial Tumors
Neuronal and mixed neuronal-glial tumors are types of rare tumors that occur in the brain or spinal cord. There are many kinds of these tumors. But a person will have just 1 tumor of 1 type.
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Campylobacter Infection in Children
Campylobacter infection is a mild to serious digestive illness. It is caused by bacteria. Symptoms often include cramping, diarrhea, belly pain, and fever.
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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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Craniopharyngioma in Children
Craniopharyngioma is a benign brain tumor that is found near the pituitary gland.
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Congenital Liver Defects
Congenital liver defects are liver disorders that are present at birth. They are rare. These liver disorders often block the bile ducts. This affects the flow of bile.
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Showing 5257 - 5265 of 12459 results