Pediatric Neurology
Volume 25, Issue 4 , Pages 328-331 , October 2001

Magnetic resonance imaging in three children with kernicterus

  • Seiichi Sugama, MD

      Affiliations

    • Corresponding Author InformationCommunications should be addressed to Dr. Sugama; Department of Pediatrics; The Jikei University School of Medicine; 3-25-8 Nishishinbashi, Minato-ku; Tokyo 105-8461, Japan
    • Department of Pediatrics, Tokyo Metropolitan Kita Medical Rehabilitation Center for Handicapped Johnan Branch, Tokyo, Japan
    • Department of Pediatrics, Tokyo Metropolitan Maternity and Child Health Institute, Tokyo, Japan
    • Department of Pediatrics, The Jikei University School of Medicine, Tokyo, Japan
  • ,
  • Atsuhiro Soeda, MD

      Affiliations

    • Department of Pediatrics, Tokyo Metropolitan Maternity and Child Health Institute, Tokyo, Japan
    • Department of Pediatrics, The Jikei University School of Medicine, Tokyo, Japan
  • ,
  • Yoshikatsu Eto, MD, PhD

      Affiliations

    • Department of Pediatrics, The Jikei University School of Medicine, Tokyo, Japan

Received 17 January 2001 ,Accepted 4 May 2001.

References 

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  2. Penn AA, Enzmann DR, Hahn JS, Stevenson DK. Kernicterus in a full term infant. Pediatrics. 1994;93:1003–1006
  3. Yokochi K. Magnetic resonance imaging in children with kernicterus. Acta Paediatr. 1995;84:937–939
  4. Martich-Kriss V, Kollias SS, Ball WS. MR findings in kernicterus. AJNR Am J Neuroradiol. 1995;16:819–821
  5. Worley G, Erwin CW, Goldstein RF, Provenzale JM, Ware RE. Delayed development of sensorineural hearing loss after neonatal hyperbilirubinemia (A case report with brain magnetic resonance imaging). Dev Med Child Neurol. 1996;38:271–278
  6. Steinborn M, Seelos KC, Heuck A, von Voss H, Reiser M. MR findings in a patient with kernicterus. Eur Radiol. 1999;9:1913–1915
  7. Hansen TWR, Bratlid D. Bilirubin and bilirubin toxicity. Acta Pediatr Scand. 1986;75:513–522
  8. Lyon G, Adams RD, Kolodny EH. Distinction between hereditary metabolic diseases and other diseases of the child’s nervous system. Kernicterus. In:  Lyon G,  Adams RD,  Kolodny EH editor. Neurology of hereditary metabolic diseases of children. 2nd ed.. New York: McGraw Hill; 1996;p. 282–285
  9. Stoll BJ, Kliegman RM. Digestive system disorders. Kernicterus. In:  Behrman RE,  Kliegman RM,  Jenson HB editor. Nelson textbook of pediatrics. 16th ed. Philadelphia: WB Saunders Company; 1995;p. 517–519
  10. Friede RL. Kernicterus (bilirubin encephalopathy). In:  Friede RL editors. Developmental neuropathology. 2nd ed.. Berlin: Springer-Verlag; 1989;p. 117–124
  11. Hayashi M, Satoh J, Sakamoto K, Morimatsu Y. Clinical and neuropathological findings in severe athetoid cerebral palsy (A comparative study of globo-Luysian and thalamo-putaminal groups). Brain Dev. 1991;13:47–51
  12. Yokochi K, Aiba K, Kodama M, Fujimoto S. Magnetic resonance imaging in athetotic cerebral palsied children. Acta Paediatr Scand. 1991;80:818–823
  13. Barkovich AJ. MR and CT evaluation of profound neonatal and infantile asphyxia. Am J Neuroradiol. 1992;13:959–972
  14. Johnson WH, Angara V, Baumal R, et al.  Erythroblastosis fetalis and hyperbilirubinemia, a five-year follow-up with neurological, psychological, and audiological evaluation. Pediatrics. 1967;39:88–92
  15. Filloux FM. Neuropathophysiology of movement disorders in cerebral palsy. J Child Neurol. 1996;11(Suppl 1):S5–S12

PII: S0887-8994(01)00306-X

Pediatric Neurology
Volume 25, Issue 4 , Pages 328-331 , October 2001