Presentation and management of classical urea cycle disorders: lessons from our experience


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KALKAN UÇAR S. , CANDA E. , KÖSE M., Kaginici M., ALTUN KÖROĞLU Ö. , ÇALKAVUR S., ...Daha Fazla

IZMIR DR BEHCET UZ COCUK HASTANESI DERGISI, cilt.6, ss.89-96, 2016 (ESCI İndekslerine Giren Dergi) identifier

  • Cilt numarası: 6 Konu: 2
  • Basım Tarihi: 2016
  • Doi Numarası: 10.5222/buchd.2016.089
  • Dergi Adı: IZMIR DR BEHCET UZ COCUK HASTANESI DERGISI
  • Sayfa Sayıları: ss.89-96

Özet

Objective: The urea cycle disorders (UCD) are inherited deficiencies of the enzymes or transport molecules involved in the cellular excretion of excess ammonia produced during protein metabolism. The aim of this study was to evaluate the clinical characteristics and long-term outcome of pediatric patients with UCD seen during childhood.