Citrullinemia in a newborn: a case report

G. Golosnaya, T. N. Belousova, M. Novikov, N. Knyazeva, D. Y. Podkopaev, E. G. Trifonova, A. I. Makulova, Ya. Ya. Ginen, Z. A. Kozheurova, D. A. Kholichev, D. A. Politov, P. V. Baranova, N. A. Ermolenko, O. Krasnorutskaya, E. Y. Kaledina, G. P. Tukabaev, A. V. Ogurtsov, K. A. Seleznev
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Abstract

Inherited metabolic disorders have a specific place among cases of sudden deterioration of the newborn’s condition. Therapies have been developed for some of these disorders. Accurate verification of the diagnosis is extremely important for choosing an optimal treatment strategy. However, treatment is not always successful due to the rapid progression of symptoms. We report a case of citrullinemia diagnosed in a newborn in Vidnoye Perinatal Center.
新生儿瓜氨酸血症1例报告
遗传性代谢紊乱在新生儿状况突然恶化的病例中占有特殊地位。针对其中一些疾病已经开发出了治疗方法。准确的诊断验证对于选择最佳治疗策略至关重要。然而,由于症状的迅速发展,治疗并不总是成功的。我们报告一个病例瓜氨酸血症诊断在一个新生儿在维德诺耶围产期中心。
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