nevoid basal cell carcinoma syndrome meaning in Chinese
痣样基底细胞癌综合征
Examples
- Recently , insight into the molecular origins of bccs came from the identification of mutations in the patched gene ( ptch ) in patients with nevoid basal cell carcinoma syndrome
( ptch )的突变，对基底细胞瘤的发生开始有了更深了解。正常情况下， - When ptch has been inactivated by mutation in nevoid basal cell carcinoma syndrome , smoothened is turned on continuously , providing a continuous signal to the cell to grow
基因由于突变而失活时，圆滑蛋白则不断地被激活，提供持续的基底细胞生长信号。 - Nevoid basal cell carcinoma syndrome , also known as gorlin syndrome , is an autosomal dominant inherited disorder which is characterized by the presence of multiple maxillary keratocysts , facial basal cell carcinomas and kinds of musculo - skeletal disturbances
摘要痣样基底细胞癌综合征是一种罕见的常染色体显性遗传疾病，以颌骨多发性角化囊肿，皮肤痣样基底细胞癌及多种骨骼异常为主要临床表现。 - Bccs usually arise in elderly light - skinned people as sporadic tumors , but are also a major feature of the nevoid basal cell carcinoma syndrome , an unusual genetic disorder characterized primarily by cancer susceptibility and some embryonic abnormalities
这种癌症在浅肤色的年长者中，常以散发性肿瘤表现出来，它也是痣样基底细胞瘤综合病徵的主要徵状，痣样基底细胞瘤是一种特别的遗传疾病，主要以癌症易感性及胚胎异常为特徵。