Infantile spasms: review of the literature and personal experience

被引:23
作者
Fois, Alberto [1 ]
机构
[1] Univ Siena, Inst Pediat Clin, I-53100 Siena, Italy
关键词
DOSE ACTH THERAPY; WEST-SYNDROME; PROGRESSIVE ENCEPHALOPATHY; EPILEPTIC ENCEPHALOPATHY; PYRIDOXAL-PHOSPHATE; MENTAL-RETARDATION; SURGICAL-TREATMENT; OHTAHARA-SYNDROME; KETOGENIC DIET; ARX GENE;
D O I
10.1186/1824-7288-36-15
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
This epileptic disorder has become a classic topic for neuropediatricians and the interest is documented by the large number of publications on this subject. The relative frequency among the epileptic syndromes is an another reason why not only neuropediatricians but also general pediatricians must be fully informed about diagnostic, clinical, imaging and genetic aspects. Early diagnosis is of paramount importance in order to obtain even complete results in patients with so called idiopathic situations. A number of problems are still to be solved. There is no agreement on the type and the schedule of treatment. A common denominator about this problem is not jet available even if some advances in this regard have been accomplished. Of paramount importance is an accurate clinical and laboratory examination as a prerequisite regarding prognosis and results of therapy in every single case. However, even if more than 170 years have elapsed since the first communication of dr. West on the peculiar syndrome that his child was suffering of, the interest of scientists on this subject has now been enriched and rewarded.
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页数:10
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