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J Med Screen ; 10(1): 2-4, 2003.
Article in English | MEDLINE | ID: mdl-12790307

ABSTRACT

The screening of newborn babies for congenital hypothyroidism has changed the natural history of this abnormality. We describe here a case of a female patient with congenital hypothyroidism that was missed by primary neonatal thyroid screening (using thyroid-stimulating hormone) at two days of age; it was detected only after the development and persistence of jaundice during the first three weeks of life. A normal neonatal screening result does not preclude the development of hypothyroidism later in infancy. Clinical vigilance must be maintained by practitioners. A second screening between two and six weeks of age may be useful in order to detect the few cases missed at first screening.


Subject(s)
Hypothyroidism/diagnosis , Neonatal Screening/methods , Thyroid Function Tests , Thyrotropin/blood , False Negative Reactions , Female , Humans , Hypothyroidism/prevention & control , Infant, Newborn , Neonatal Screening/standards , Reproducibility of Results
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