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1.
Eur J Neurol ; 17(6): 815-22, 2010 Jun 01.
Article in English | MEDLINE | ID: mdl-20113335

ABSTRACT

INTRODUCTION: Neuroimaging of the brain in the diagnostic work-up of patients with neurodevelopmental disorders is a matter of continuing debate. Recommendations range from performing brain imaging in all patients with neurodevelopmental disorders to performing an MRI only in those with indication on clinical examinations. Important indications for neuroimaging are head size abnormalities and focal neurological findings. METHODS: Patients with neurodevelopmental disorders of unknown origin (n = 410), referred to a specialized tertiary diagnostic center for neurodevelopmental disorders were included in a retrospective analysis. A 1-day work-up, including an MRI of the brain was performed. Studied were the: (i) yield of MRI scans of the brain and (ii) associations of specific clinical symptoms/signs with abnormal and diagnostic MRI scans. RESULTS: (i) In 30.7% of the 410 patients with neurodevelopmental disorders (n = 126), abnormal MRI scans were observed, leading to an etiological diagnosis in 5.4% of the patients (n = 22). (ii) Pyramidal disorders (P = 0.001), epilepsy (P = 0.04) and an abnormal head circumference (P = 0.02) were associated with an abnormal MRI scan. The presence of one of the following neurological symptoms/signs: movement disorders, pyramidal disorders, epilepsy, or an abnormal head circumference was associated with a diagnostic MRI scan (P < 0.001) (diagnostic MRI % in neurological versus no neurological symptoms/signs, 13.0% versus 1.9%). CONCLUSION: Neuroimaging of the brain in a tertiary care center for patients with neurodevelopmental disorders of unknown origin is useful, especially in case of neurological symptoms/signs.


Subject(s)
Brain/pathology , Developmental Disabilities/diagnosis , Magnetic Resonance Imaging , Adolescent , Child , Child, Preschool , Female , Humans , Infant , Male , Retrospective Studies
2.
J Inherit Metab Dis ; 28(6): 1151-2, 2005.
Article in English | MEDLINE | ID: mdl-16435213

ABSTRACT

A patient with very long-chain acyl-CoA dehydrogenase (VLCAD) deficiency presented in the neonatal period with hypoketotic hypoglycaemia and at the age of 1 year with rhabdomyolysis and normal glucose after fasting. Rhabdomyolysis may occur in the absence of hypoglycaemia in young infants as well as in older patients.


Subject(s)
Acyl-CoA Dehydrogenase, Long-Chain/deficiency , Blood Glucose/metabolism , Metabolism, Inborn Errors/complications , Rhabdomyolysis/complications , Carnitine/analogs & derivatives , Carnitine/blood , Fasting , Glucose/metabolism , Humans , Hypoglycemia/complications , Hypoglycemia/diagnosis , Infant , Metabolism, Inborn Errors/diagnosis , Rhabdomyolysis/diagnosis
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