| Literature DB >> 12790307 |
K A Yunis1, M R Nasr, G Lepejian, S Najjar, R Daher.
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.Entities:
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Year: 2003 PMID: 12790307 DOI: 10.1258/096914103321610725
Source DB: PubMed Journal: J Med Screen ISSN: 0969-1413 Impact factor: 2.136