경련을 동반한 신생아 부신백질이영양증

Neonatal Adrenoleukodystrophy Presenting with Neonatal Seizure

  • 신영림 (울산대학교 의과대학 서울아산병원 소아과) ;
  • 유한욱 (울산대학교 의과대학 서울아산병원 소아과)
  • Shin, Young-Lim (Department of Pediatrics, Asan Medical Center, College of Medicine, University of Ulsan) ;
  • Yoo, Han-Wook (Department of Pediatrics, Asan Medical Center, College of Medicine, University of Ulsan)
  • 발행 : 2002.07.05

초록

Disorders resulting from defects in peroxisomal biogenesis include Zellweger syndrome, neonatal adrenoleukodystrophy, and infantile Refsum disease. The three diseases are now considered as a continuum of clinical features. Neonatal adrenoleukodystrophy is intermediate between Zellweger syndrome and infantile Refsum disease in severity, and is characterized by profound hypotonia, intractable seizures and premature death. We report a cases of neonatal adrenoleukodystrophy presenting with neonatal seizure and hypotonia. At the age of 43 months, she had clinical evidence of adrenal insufficiency with skin hyperpigmentation and electrolyte imbalance. She was diagnosed having neonatal adrenoleukodystrophy based on abnormally high levels of plasma very long-chain fatty acids, pipecolic acid and phytanic acid.

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