着色性干皮症 Xeroderma pigmentosum
着色性干皮症(Xeroderma pigmentosum, XP)是一种遗传性疾病。患者皮肤细胞被阳光中的紫外线破坏之后不能自行修复,于儿童期即很易诱发癌变。发病率为1/25万。
单词 | Xeroderma pigmentosa |
释义 |
Xeroderma pigmentosa
中文百科
着色性干皮症 Xeroderma pigmentosum(重定向自Xeroderma pigmentosa)
着色性干皮症(Xeroderma pigmentosum, XP)是一种遗传性疾病。患者皮肤细胞被阳光中的紫外线破坏之后不能自行修复,于儿童期即很易诱发癌变。发病率为1/25万。
英语百科
Xeroderma pigmentosum 着色性乾皮症(重定向自Xeroderma pigmentosa)
![]() ![]() ![]() ![]() Xeroderma pigmentosum (XP) is a rare autosomal recessive genetic disorder of DNA repair in which the ability to repair damage caused by ultraviolet (UV) light is deficient. In extreme cases, all exposure to sunlight must be forbidden, no matter how small; as such, individuals with the disease are often colloquially referred to as "Moon child". Multiple basal cell carcinomas (basaliomas) and other skin malignancies frequently occur at a young age in those with XP; metastatic malignant melanoma and squamous cell carcinoma are the two most common causes of death in XP victims. This disease involves both sexes and all races, with an incidence of 1:250,000 in the United States. XP is roughly six times more common in Japanese people than in other groups. |
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