Rett syndrome and anesthetic management Rett sendromu ve anestezi yönetimi

Çevikkalp E., Gül Hayran G., TEZCAN KELEŞ G.

Anestezi Dergisi, cilt.25, sa.3, ss.159-162, 2017 (Scopus) identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 25 Sayı: 3
  • Basım Tarihi: 2017
  • Dergi Adı: Anestezi Dergisi
  • Derginin Tarandığı İndeksler: Scopus, TR DİZİN (ULAKBİM)
  • Sayfa Sayıları: ss.159-162
  • Anahtar Kelimeler: Aryhtmia, Difficult airway, Malign hyperthermia, Respiratory distress, Rett syndrome
  • Manisa Celal Bayar Üniversitesi Adresli: Evet

Özet

Rett syndrome is a developmental and neurological disease characterized by defective X and is caused by mutations in the gene MECP2 coded chromosomes. It is a central involvement diesase that starts in the early developmental years, together along with EEG abnormalities, seizures, mental retardation. Orthopedic, respiratory and cardiac problems can also be seen. Prolonged QT, scoliosis, apnea, cachexia is common in children with this syndrome and requires significant anesthesia care and attention. In this case, we emphasized the anesthetic management of a Rett Syndrome child, its possible risks and problems.