Incontinentia pigmenti is a rare genodermatosis that usually affects female infants.The associated abnormalities involve ocular, dental, skeletal and central nervous systems.

色素失禁症是一种罕见皮肤遗传，常发生在女性，除了皮肤以外还可出现眼睛，牙齿，骨骼，以及中枢神经异常。

Rows of vesicles over erythematous bases are the typical cutaneous lesions of the first stage of incontinentia pigmenti (IP).

摘要第一期色素失禁症典型皮肤临床表现是一整排水泡加上红色基底。