瓜氨酸血症
医学
尿素循环
儿科
内科学
遗传学
精氨酸
氨基酸
生物
作者
Mustafa Kılıç,Esma Altınel-Açoğlu,Pelin Zorlu,Deniz Yüksel,Selda Bülbül,Johannes Haeberle
标识
DOI:10.24953/turkjped.2017.06.013
摘要
Kılıç M, Altınel-Açoğlu 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.
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