Literature DB >> 19287347

Intellectual, adaptive, and behavioral functioning in children with urea cycle disorders.

Lauren Krivitzky1, Talin Babikian, Hye-Seung Lee, Nina Hattiangadi Thomas, Karen L Burk-Paull, Mark L Batshaw.   

Abstract

Inborn errors of urea synthesis lead to an accumulation of ammonia in blood and brain and result in high rates of mortality and neurodevelopmental disability. This study seeks to characterize the cognitive, adaptive, and emotional/behavioral functioning of children with urea cycle disorders (UCDs). These domains were measured through testing and parent questionnaires in 92 children with UCDs [33 neonatal onset (NO), 59 late onset (LO)]. Results indicate that children who present with NO have poorer outcome than those who present later in childhood. Approximately half of the children with NO performed in the range of intellectual disability (ID), including a substantial number ( approximately 30%) who were severely impaired. In comparison, only a quarter of the LO group was in the range of ID. There is also evidence that the UCD group has difficulties in aspects of emotional/behavioral and executive skills domains. In conclusion, children with UCDs present with a wide spectrum of cognitive outcomes. Children with NO disease have a much higher likelihood of having an ID, which becomes even more evident with increasing age. However, even children with LO UCDs demonstrate evidence of neurocognitive and behavioral impairment, particularly in aspects of attention and executive functioning.

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Year:  2009        PMID: 19287347      PMCID: PMC2746951          DOI: 10.1203/PDR.0b013e3181a27a16

Source DB:  PubMed          Journal:  Pediatr Res        ISSN: 0031-3998            Impact factor:   3.756


  21 in total

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9.  Cerebral dysfunction in asymptomatic carriers of ornithine transcarbamylase deficiency.

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Journal:  N Engl J Med       Date:  1980-02-28       Impact factor: 91.245

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Authors:  S W Brusilow; D L Valle; M Batshaw
Journal:  Lancet       Date:  1979-09-01       Impact factor: 79.321

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5.  Favorable long-term outcome following severe neonatal hyperammonemic coma in a patient with argininosuccinate synthetase deficiency.

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6.  Diffusion tensor imaging detects areas of abnormal white matter microstructure in patients with partial ornithine transcarbamylase deficiency.

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Review 7.  A longitudinal study of urea cycle disorders.

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Journal:  Mol Genet Metab       Date:  2014-08-10       Impact factor: 4.797

8.  Early liver transplantation in neonatal-onset and moderate urea cycle disorders may lead to normal neurodevelopment.

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9.  Clinical outcomes of neonatal onset proximal versus distal urea cycle disorders do not differ.

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Journal:  Hepatology       Date:  2013-01-03       Impact factor: 17.425

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