Metabolic and genetic disorders mimicking cerebral palsy
نویسندگان
چکیده
منابع مشابه
Cerebral Palsy: Motor Types, Gross Motor Function and Associated Disorders
Objectives: Cerebral palsy (CP) describes a group of disorders in the development of movement and posture in the developing brain. The main aim of this study was to determine the distribution of motor impairment and associated disorders in a population of children with CP. Methods: This study was carried out in 2011 during three months, on 200 CP children. Multiple sources of ascertainment w...
متن کاملGlutaric Aciduria Type I: A Rare Metabolic Disorder Mimicking as Choreoathetoid Cerebral Palsy
Glutaric aciduria type I (GA I) is an autosomal recessive inborn error of metabolism caused by a deficiency of the enzyme glutaryl-CoA dehydrogenase. This disorder is characterized by progressive dystonia, choreoathetosis, and dyskinesia. It is often misdiagnosed as athetoid cerebral palsy. Laboratory evaluation usually demonstrates increased urinary excretion of gluataric acid and 3-hydroxyglu...
متن کاملcerebral palsy: motor types, gross motor function and associated disorders
objectives: cerebral palsy (cp) describes a group of disorders in the development of movement and posture in the developing brain. the main aim of this study was to determine the distribution of motor impairment and associated disorders in a population of children with cp. methods: this study was carried out in 2011 during three months, on 200 cp children. multiple sources of ascertainment were...
متن کاملParental age, genetic mutation, and cerebral palsy.
Parental age and birth order were studied in 251 patients with cerebral palsy. No parental age or birth order effects were observed in spastic quadriplegia or diplegia, but a paternal age effect was detected in those with athetoid/dystonic cerebral palsy and congenital hemiplegia. These observations indicate that some cases of athetoid/dystonic or hemiplegic cerebral palsy might arise by fresh ...
متن کاملAtaxic cerebral palsy and genetic predisposition.
It was calculated that in the 962 family members of 36 patients with ataxic cerebral palsy there were 75 (8%) with a history of neurodevelopmental disorder and 31 (3%) with a major congenital malformation. This was not significantly greater than expected, and does not support the hypothesis of a genetic non-Mendelian role in the aetiology of ataxic cerebral palsy.
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ژورنال
عنوان ژورنال: Neurosciences
سال: 2019
ISSN: 1658-3183
DOI: 10.17712/nsj.2019.3.20190045