本文關(guān)鍵詞： 伊藤色素減少癥 線狀痣 色素失禁 中樞神經(jīng)系統(tǒng) 色素性 無色素痣 色素減退 萊昂化作用 足月順產(chǎn) 個月　出處：《重慶醫(yī)學》2017年28期 　論文類型：期刊論文

【摘要】：正伊藤色素減少癥(hypomelanosis of Ito,HI)也叫做線狀痣樣色素減退、色素鑲嵌癥或無色素性色素失禁[1]。HI可累及多重系統(tǒng),包括中樞神經(jīng)系統(tǒng)、骨骼、肌肉和眼等。當累及中樞神經(jīng)系統(tǒng)時常表現(xiàn)為癲癇發(fā)作。該病為罕見病,本文對1例伊藤色素減少癥并發(fā)癲癇的患兒進行綜合剖析,為今后診治的工作提供參考。1臨床資料患兒,女,10個月22天,系第1胎第1產(chǎn),足月順產(chǎn),新法
[Abstract]:Hypomelanosis of Itohithia) is also known as linear nevus pigmentation, pigment mosaic or achromatic incontinence [1] .HI can involve multiple systems, including the central nervous system, bone, and bone. When the central nervous system is involved, epilepsy often occurs. The disease is a rare disease. A case of Itochromocytopenia complicated with epilepsy was analyzed in this paper. To provide reference for future diagnosis and treatment of children with clinical data, female, 10 months 22 days, is the first birth of the first birth, full birth, new method
【作者單位】： 廣西醫(yī)科大學第二附屬醫(yī)院神經(jīng)內(nèi)科;
【分類號】：R725.9;R742.1
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本文編號：1542731