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Jaundice associated with high levels of unconjugated bilirubin, or in small premature infants with more modest degrees of bilirubinemia; yellow staining and degenerative lesions are found chiefly in basal ganglia including in the lenticular nucleus, subthalamus, Ammon horn, and other areas; may occur with hemolytic disorder such as Rh or ABO erythroblastosis or G6PD deficiency as well as with neonatal sepsis or Crigler-Najjar syndrome; characterized early clinically by opisthotonus, high-pitched cry, lethargy, and poor sucking, as well as abnormal or absent Moro reflex, and loss of upward gaze; later consequences include deafness, cerebral palsy, other sensineural deficits, and mental retardation. SYN: bilirubin encephalopathy, nuclear jaundice. [Ger. Kern, kernel (nucleus), + Ikterus, jaundice]
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ker·nic·ter·us kər-'nik-tə-rəs n a condition marked by the deposit of bile pigments in the nuclei of the brain and spinal cord and by degeneration of nerve cells that occurs usu. in infants as a part of the syndrome of erythroblastosis fetalis
ker·nic·ter·ic -rik adj
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n.
staining and subsequent damage of the brain by bile pigment (bilirubin), which may occur in severe cases of haemolytic disease of the newborn. Immature brain cells in the basal ganglia are affected, and as brain development proceeds a pattern of cerebral palsy emerges at about six months, with uncoordinated movements, deafness, disturbed vision, and feeding and speech difficulties.
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ker·nic·ter·us (kər-nikґtər-əs) [Ger. “nuclear jaundiceâ€] a condition associated with high levels of bilirubin in the blood, nearly always with severe neural symptoms, usually seen in infants as a sequela of icterus gravis neonatorum. It is characterized by deep yellow staining of the basal nuclei, globus pallidus, putamen, caudate nucleus, cerebellar nuclei, bulbar nuclei, and gray substance of the cerebrum, accompanied by widespread destructive changes. Called also bilirubin encephalopathy.Medical dictionary. 2011.