Vitamin-Responsive Movement Disorders in Children

被引:3
作者
Sondhi, Vishal [1 ]
Sharma, Suvasini [2 ]
机构
[1] Armed Forces Med Coll, Dept Pediat, Pune, Maharashtra, India
[2] Lady Hardinge Med Coll & Hosp, Dept Pediat, New Delhi 110001, India
关键词
Biotin-thiamine-responsive basal ganglia disease; biotinidase deficiency; inherited metabolic disorders; DEFICIENCY; DISEASE; BIOTIN; MUTATIONS; INFANTS; FOLATE; ATAXIA;
D O I
10.4103/aian.AIAN_678_19
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Movement disorders in childhood comprise a heterogeneous group of conditions that lead to impairment of voluntary movement, abnormal postures, or inserted involuntary movements. Movement disorders in children are frequently caused by metabolic disorders, both inherited and acquired. Many of these respond to vitamin supplementation. Examples include infantile tremor syndrome, biotinidase deficiency, biotin-thiamine-responsive basal ganglia disease, pyruvate dehydrogenase deficiency, aromatic amino acid decarboxylase deficiency, ataxia with vitamin E deficiency, abetalipoproteinemia, cerebral folate deficiency, and cobalamin metabolism defects. Recognition of these disorders by pediatricians and neurologists is imperative as they are easily treated by vitamin supplementation. In this review, we discuss vitamin-responsive movement disorders in children.
引用
收藏
页码:325 / 331
页数:7
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