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A 14-year-old girl with an unusual combination of incontinentia pigmenti and conversion disorder

机译:一名14岁女孩患有色素失禁和转换障碍的异常组合

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摘要

Incontinentia pigmenti is a rare X-linked neurological-skin genetic disease. Some studies have shown that about 30~40% of patients with IP have varying symptoms of eye/central nervous system which are the major causes of disability. Conversion disorder is one of the most common mental diseases in children and may exhibit the single or multiple neurological symptoms. In this paper, we will report a child with new and rare incontinentia pigmenti accompanied by conversion disorder and explore the relationship of this rare combination.
机译:色素失禁是一种罕见的X连锁神经皮肤遗传病。一些研究表明,大约30%至40%的IP患者的眼睛/中枢神经系统症状多种多样,是导致残疾的主要原因。转换障碍是儿童中最常见的精神疾病之一,可能表现出单一或多种神经系统症状。在本文中,我们将报告一名患有新的和罕见的色素失禁性尿失禁伴有转化障碍的儿童,并探讨这种罕见组合的关系。

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