头发颜色可以是某些疾病(色素沉着不足)的生物标志物,因此了解一些基于遗传的临床特征的地理分布非常重要。
全身色素沉着障碍。

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1.
Tey H. 儿童色素沉着不足疾病的实用分类。 Acta Derm Venerol [互联网]。 2010 年 [2023 年 3 月 1 日引用];90(1):6–11。可从: https://medicaljournalssweden.se/actadv/article/view/7578
MC1R 突变。 北欧红发.



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1.
红头发的遗传原因、种族起源和历史 - Eupedia [互联网]。 2023 年 [引自 2023 年 3 月 1 日]。可从: https://www.eupedia.com/genetics/origins_of_red_hair.shtml
在眼皮肤白化病中,根据酶缺乏的强度和潜在的遗传问题,可能会有不同深浅的颜色,变成红色或棕色头发,因此表型谱非常广泛。


白化病。
有一组综合征产生与眼皮肤白化病相似的表型,并且是与其鉴别诊断的一部分。
- 赫曼斯基-普德拉克综合征。
- 切迪亚克-东综合征。
- Angelman和Prader-Willi综合征。
- 维西综合症。
- 格里塞利综合征。
获得性发色障碍。

局灶性色素沉着不足的疾病。

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