Your browser doesn't support javascript.
loading
First manifestation of citrullinemia type I as Sandifer syndrome.
Kiliç, Mustafa; Altinel-Açoglu, Esma; Zorlu, Pelin; Yüksel, Deniz; Bülbül, Selda; Haeberle, Johannes.
Affiliation
  • Kiliç M; Divisions of Metabolism, Dr. Sami Ulus Children Hospital, Ankara, Turkey.
  • Altinel-Açoglu E; Department of Pediatrics, Dr. Sami Ulus Children Hospital, Ankara, Turkey.
  • Zorlu P; Department of Pediatrics, Dr. Sami Ulus Children Hospital, Ankara, Turkey.
  • Yüksel D; Pediatric Neurology, Dr. Sami Ulus Children Hospital, Ankara, Turkey.
  • Bülbül S; Department of Pediatric Metabolism, Kirikkale University, Faculty of Medicine, Kirikkale, Turkey.
  • Haeberle J; Division of Metabolism and Children's Research Center, University Children's Hospital, Zurich, Switzerland.
Turk J Pediatr ; 59(6): 696-698, 2017.
Article in En | MEDLINE | ID: mdl-30035404
Kiliç M, Altinel-Açoglu E, Zorlu P, Yüksel D, Bülbül S, Haeberle J. First manifestation of citrullinemia type I as Sandifer syndrome. Turk J Pediatr 2017; 59: 696-698. We report an eleven-month-old infant girl who presented as Sandifer syndrome clinically but was later diagnosed with citrullinemia type I. Metabolic evaluation and molecular analysis confirmed the correct diagnosis. Despite the fact that many patients are already known in the literature, this is the first report of a Sandifer syndrome-like presentation of citrullinemia type I. This paper suggests that suspicion of Sandifer syndrome should also lead to inclusion of urea cycle disorders in the list of differential diagnoses.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Turk J Pediatr Year: 2017 Document type: Article Affiliation country: Turquía Country of publication: Turquía

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Turk J Pediatr Year: 2017 Document type: Article Affiliation country: Turquía Country of publication: Turquía