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1.
J Inherit Metab Dis ; 29(6): 701-4; discussion 705-6, 2006 Dec.
Article in English | MEDLINE | ID: mdl-17041745

ABSTRACT

The blood-brain barrier (BBB) metabolically isolates the central nervous system (CNS) from the circulation and protects it against fluctuations of hydrophilic nutrients in plasma and from intoxication. Recent studies have shown that dicarboxylic acids (DCAs) are transported across the blood-brain barrier at very low rates. In organic acidaemias, neurological complications are common. We hypothesize that, as a result of the very limited efflux, in certain organic acidaemias there is pathological accumulation of DCAs (e.g. glutarate, 3-hydroxyglutarate, D-2- and L-2-hydroxyglutarate, methylmalonate) in the brain secondary to the metabolic block. At high concentrations some of these compounds may become neurotoxic. Treatment should be aimed at preventing the accumulation of these compounds using our understanding of the properties of the BBB.


Subject(s)
Blood-Brain Barrier , Metabolism, Inborn Errors/complications , Metabolism, Inborn Errors/diagnosis , Nervous System Diseases/complications , Organic Anion Transporters/metabolism , Animals , Biological Transport , Brain/pathology , Central Nervous System/pathology , Humans
2.
Arch Dis Child ; 89(7): 604-10, 2004 Jul.
Article in English | MEDLINE | ID: mdl-15210487

ABSTRACT

BACKGROUND: The classical extrapyramidal movement disorder following beta haemolytic streptococcus (BHS) infection is Sydenham's chorea (SC). Recently, other post-streptococcal movement disorders have been described, including motor tics and dystonia. Associated emotional and behavioural alteration is characteristic. AIMS: To describe experience of post-streptococcal dyskinesias and associated co-morbid psychiatric features presenting to a tertiary referral centre 1999-2002. METHODS: In all patients, dyskinetic movement disorders followed BHS pharyngeal infection. BHS infection was defined by pharyngeal culture of the organism, or paired streptococcal serology. Movement disorders were classified according to international criteria, and validated by experienced child neurologists. Psychiatric complications were defined using ICD-10 criteria using a validated psychiatric interview. RESULTS: In the 40 patients, the following dyskinetic movement disorders were present: chorea (n = 20), motor tics (n = 16), dystonia (n = 5), tremor (n = 3), stereotypies (n = 2), opsoclonus (n = 2), and myoclonus (n = 1). Sixty five per cent of the chorea patients were female, whereas 69% of the tic patients were male. ICD-10 psychiatric diagnoses were made in 62.5%. Using the same psychiatric instrument, only 8.9% of UK children would be expected to have an ICD-10 psychiatric diagnosis. Emotional disorders occurred in 47.5%, including obsessive-compulsive disorder (27.5%), generalised anxiety (25%), and depressive episode (17.5%). Additional psychiatric morbidity included conduct disorders (27.5%) and hyperkinetic disorders (15%). Psychiatric, movement, and post-streptococcal autoimmune disorders were commonly observed in family members. At a mean follow up of 2.7 years, 72.5% had continuing movement and psychiatric disorders. CONCLUSION: Post-streptococcal dyskinesias occur with significant and disabling psychiatric co-morbidity and are potential autoimmune models of common "idiopathic" movement and psychiatric disorders in children. Multiple factors may be involved in disease expression including genetic predisposition, developmental status, and the patient's sex.


Subject(s)
Dyskinesias/microbiology , Mental Disorders/microbiology , Streptococcal Infections/complications , Adolescent , Child , Child Behavior Disorders/microbiology , Child, Preschool , Dyskinesias/psychology , Family Health , Female , Humans , Hyperkinesis/microbiology , Infant , Male , Mood Disorders/microbiology , Prognosis , Psychiatric Status Rating Scales , Streptococcal Infections/psychology
3.
Neurology ; 62(10): 1872-4, 2004 May 25.
Article in English | MEDLINE | ID: mdl-15159499

ABSTRACT

Two girls and one boy are described, with severe infantile parkinsonism-dystonia. This syndrome is usually caused by endogenous dopamine deficiency but in these patients was associated with elevated dopamine metabolites in CSF and an unusual eye movement disorder: ocular flutter together with saccade initiation failure. Pyramidal tract signs also emerged in the course of the disease in two patients. This combination of symptoms and biochemical findings suggests a unique pathogenic mechanism.


Subject(s)
Dopamine/cerebrospinal fluid , Dystonic Disorders/cerebrospinal fluid , Homovanillic Acid/cerebrospinal fluid , Ocular Motility Disorders/cerebrospinal fluid , Parkinson Disease/cerebrospinal fluid , Dopamine/urine , Dystonic Disorders/diagnostic imaging , Female , Homovanillic Acid/urine , Humans , Hydroxyindoleacetic Acid/cerebrospinal fluid , Infant, Newborn , Male , Ocular Motility Disorders/diagnostic imaging , Parkinson Disease/diagnostic imaging , Reflex, Abnormal , Saccades , Syndrome , Tomography, Emission-Computed, Single-Photon
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