欧洲色素失禁症患者的诊断和实践管理共识解读

2021-10-25 中国循证医学杂志

色素失禁症(incontinentia pigmenti,IP)是一种罕见的X染色体连锁显性遗传病,具有特征性的皮损表现。该病在婴儿期即可发病,且容易被误诊,并可能伴随严重的眼部和/或脑部并发症。20

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2021-10-25

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色素失禁症(incontinentia pigmenti,IP)是一种罕见的X染色体连锁显性遗传病,具有特征性的皮损表现。该病在婴儿期即可发病,且容易被误诊,并可能伴随严重的眼部和/或脑部并发症。2020年3月欧洲罕见皮肤病网络(ERN-Skin)发布了《欧洲多学科共识建议:色素失禁症患者的诊断和实践管理》,对IP的诊断、治疗、随访等方面给出了共识建议。本文对其进行解读,以期为诊治色素失禁症提供参考。

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2021-12-19 yx1156

好文章，学习中！

62 0
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2021-12-16 微探

学习学习

0 0
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2021-12-15 ms4000000889797598

学习

66 0
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2021-12-15 ms2000000506051003

很好

68 0
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2021-12-15 630383810

非常及时

68 0

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