Am J Perinatol 2003; 20(1): 025-032
DOI: 10.1055/s-2003-37952
Copyright © 2003 by Thieme Medical Publishers, Inc., 333 Seventh Avenue, New York, NY 10001, USA. Tel.: +1(212) 584-4662

Lethal Neonatal Carnitine Palmitoyltransferase II Deficiency: An Unusual Presentation of a Rare Disorder

Renu Sharma1 , Anthony A. Perszyk2 , Donald Marangi3 , Carmela Monteiro4 , Savithri Raja5
  • 1Division of Neonatology, University of Florida Health Science Center at Jacksonville, Florida
  • 2Division of Genetics, University of Florida Health Science Center at Jacksonville, Florida
  • 3Division of Cardiology, Department of Pediatrics, University of Florida Health Science Center at Jacksonville, Florida
  • 4Department of Pathology, University of Florida Health Science Center at Jacksonville, Florida
  • 5Undergraduate, B.Sc. Microbiology, Kings College, Division of Life Sciences, University of London, London, United Kingdom
Further Information

Publication History

Publication Date:
14 March 2003 (online)

ABSTRACT

A term male newborn, appropriate for gestational age, developed hypothermia, severe cardiac dysrrhythmia, and nonoliguric hyperkalemia within 24 hours of birth. Despite the prenatal identification of cystic renal dysplasia without oligohydramnios, at birth, a solitary left leg vascular hemangioma and large palpable kidneys were the only anomalies. Gradually hypotonia, lethargy, and poor feeding developed and by 20 hours of age recurrent cardiac dysrrhythmias, myocardial dysfunction, and renal insufficiency with intermittent hyperkalemia were apparent. Episodes of apnea developed on day 7 followed by respiratory failure, recurrent cardiac dysrrhythmias, and death on day 12. Eventually laboratory and autopsy findings confirmed the diagnosis of lethal neonatal carnitine palmitoyltransferase II deficiency.

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