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Archivos argentinos de pediatría
versión impresa ISSN 0325-0075
Resumen
DEGIRMENCIOGLU, Halil et al. Citrullinemia with an atypical presentation: persistent hiccups: case report. Arch. argent. pediatr. [online]. 2014, vol.112, n.5, pp.e206-e208. ISSN 0325-0075. http://dx.doi.org/10.5546/aap.2014.e206.
We report an infant who developed encephalopathy within the first 3 days of life. He had persistent hiccups that progressed to deep coma 72 hours after admission. The sepsis parameters and cerebrospinal fluid examination (CSF) were normal. The metabolic evaluation confirmed hyperammonemia, and hypercitrullinemia. The ratio of CSF/plasma glycine concentration was normal. This did not agree with our initial diagnosis of nonketotic hyperglycinemia where hiccups is present more often. Neonatal onset of argininosuccinic acid synthetase deficiency (ASD; citrullinemia) should be brought in mind in the differential diagnosis of encephalopathy in association with hiccups in the neonatal period suggesting inborn errors of metabolism.
Palabras clave : Citrullinemia; Hiccups; Neonate.