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  Vol. 286 No. 3, July 18, 2001 TABLE OF CONTENTS
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  From the Centers for Disease Control and Prevention: Morbidity and Mortality Weekly Report
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Kernicterus in Full-Term Infants—United States, 1994-1998

JAMA. 2001;286:299-300.

Since this article does not have an abstract, we have provided the first 150 words of the full text and any section headings.

MMWR. 2001;50:491-494

Kernicterus is a preventable life-long neurologic syndrome caused by severe and untreated hyperbilirubinemia during the neonatal period. High levels of bilirubin are toxic to the developing newborn. In full-term infants, hyperbilirubinemia symptoms include severe jaundice, lethargy, and poor feeding. Features of kernicterus may include choreoathetoid cerebral palsy, mental retardation, sensorineural hearing loss, and gaze paresis. Kernicterus is not a reportable condition in the United States, and its prevalence is unknown; however, a pilot registry at a Pennsylvania hospital documented 90 cases in 21 states from 1984 to June 2001 (L. Johnson, Pennsylvania Hospital, Philadelphia, personal communication, 2001). This report summarizes case histories of four full-term, healthy infants who developed kernicterus and underscores that to prevent kernicterus, newborns must be screened and promptly treated for hyperbilirubinemia.1

In early 2001, a national support group for parents of children with kernicterus conducted a survey on kernicterus. A convenience sample of 15 . . . [Full Text of this Article]

Case 1

Case 2

Case 3

Case 4



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