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what is 'newborn screening'?

Definition for Newborn Screening

Newborn Screening is also known as: Newborn screening

Newborn Screening is a medical procedure used for such diagnoses as: galactosemia, cystic fibrosis and hypothyroidism.

related diagnosis search results for 'newborn screening'
1 - 5 of 17 diagnosis
galactosemia
inherited defect in digesting galactose
cystic fibrosis
inherited multisystem disease causing thick mucus in respiratory and digestive systems
hypothyroidism
low thyroid hormone in blood
Duchenne dystrophy
inherited muscle disease beginning in legs and affecting entire body
congenital adrenal hyperplasia
inherited deficiency of adrenal hormones
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web search results for 'newborn screening'?
Results 1 - 50 - Newborn Screening
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