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Query: UMLS:C0013421 (
dystonia
)
8,418
document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)
A 4 year old girl with mild mental retardation presented with convulsions, coma and hepatomegaly. She died rapidly. The main biochemical findings were hypoglycaemia, metabolic acidosis, generalised aminoaciduria, elevation of the plasma and urine alpha-amino adipic acid, massive urine excretion of glutaric and glutaconic acids with traces of alpha-hydroxyglutaric acid. The diagnosis of glutaric aciduria was confirmed by the low activity of
glutaryl CoA dehydrogenase
in liver tissue. This diagnosis should be considered in children with progressive neurological disorders (
dystonia
, choreoathetosis) and in children with an illness similar to Reye's syndrome.
...
PMID:[Glutaric aciduria. 1 new case]. 49 39
Glutaric aciduria type 1 (GA1) is an autosomal recessive neurometabolic disorder due to
glutaryl CoA dehydrogenase
deficiency. Comprehensive descriptions of GA1-associated movement disorders are rare. In order to refine the description of the motor phenotype, we prospectively studied 16 consecutive pediatric and adult GA1 patients, focusing on the movement disorders and their time course. In most patients, generalized
dystonia
, superimposed on baseline axial hypotonia, remained the predominant feature throughout the disease course. With aging, it tended to evolve from mobile to fixed
dystonia
and to be associated with akinetic-rigid parkinsonism. Prominent orofacial involvement was a consistent feature in GA1 patients with movement disorders, resulting in speech disorders with features of combined hyperkinetic dysarthria and speech apraxia. The types and outcome of movement disorders in this setting should be taken into consideration during rehabilitation and for patient selection and evaluation in therapeutic trials.
...
PMID:Spectrum of movement disorders associated with glutaric aciduria type 1: a study of 16 patients. 1882 14