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Cystic Fibrosis Genetic Carrier Testing
This test is done to see if you carry a defective gene that may cause cystic fibrosis in your child.
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Gene Mutation for Cystic Fibrosis in Newborns (Blood)
This test looks for cystic fibrosis in newborn babies. People with CF tend to develop chronic lung disease and are at risk for lung infections.
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Cystic Fibrosis Sweat Test
A sweat chloride test is used to diagnose cystic fibrosis, a disease that causes mucus to build up in the lungs and other organs.
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Cytomegalovirus (Blood)
This test looks for antibodies to cytomegalovirus (CMV), a virus in the herpes family, in your blood.
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Cytomegalovirus (Urine)
This test looks for cytomegalovirus, a common virus that belongs to the herpes family. Your doctor might order the test if you have unexplained symptoms that are like the flu.
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Trisomy 13 and Trisomy 18 in Children
Trisomy 13 and trisomy 18 are genetic problems. They include a combination of birth defects. These include severe learning problems and health problems that affect nearly every organ in the body.
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Diphtheria in Children
A detailed look at diphtheria, including symptoms, treatment, and a vaccination schedule.
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Clubfoot in Children
Clubfoot is a deformity of the foot. It's when one or both feet are turned inward. The condition affects the bones, muscles, tendons, and blood vessels. Clubfoot is present at birth. Learn more about clubfoot in children, including what the symptoms are and how it is treated.
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Dislocations in Children
A dislocation is a joint injury. It occurs when the ends of two connected bones come apart. Dislocations happen more often among teens.
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