Kelsell D P, Stevens H P
Centre for Cutaneous Biology, St Bartholomew's and the Royal London Hospital, 2 Newark Street, London, UK E1 2AT.
Mol Med Today. 1999 Mar;5(3):107-13. doi: 10.1016/s1357-4310(98)01428-2.
The inherited palmoplantar keratodermas (PPKs) are a diverse and often clinically confusing branch of the genetic skin diseases. As the name suggests, the lesions of PPK primarily affect the palms and soles of the feet, although a number of the PPKs are also associated with a genetic predisposition to other conditions, including cancer, hearing loss and heart failure. The mapping and identification of genes that underlie the PPKs reveal new insights into the biological interactions of the structural components of the palmoplantar epidermis and further our understanding of epidermal disease. More significantly, by genetically characterizing the PPKs, genes that have a role in life-threatening disorders might also be identified.
遗传性掌跖角化病(PPK)是遗传性皮肤病中一个多样且临床症状常常令人困惑的分支。顾名思义,PPK的病变主要影响手掌和脚底,不过许多PPK还与其他病症的遗传易感性有关,包括癌症、听力丧失和心力衰竭。对导致PPK的基因进行定位和识别,为掌跖表皮结构成分的生物相互作用带来了新的见解,并加深了我们对表皮疾病的理解。更重要的是,通过对PPK进行基因特征分析,可能还会识别出在危及生命的疾病中起作用的基因。