Viana Fernanda de Oliveira, Cavaleiro Luíza Helena dos Santos, Carneiro Clívia Maria Moraes de Oliveira, Bittencourt Maraya de Jesus Semblano, Barros Renata Silva, Fonseca Diana Mendes da
Dermatology Department, Universidade Federal do Pará, Belém, PA, Brasil.
An Bras Dermatol. 2011 Sep-Oct;86(5):1029. doi: 10.1590/s0365-05962011000500033.
Xeroderma pigmentosum is a rare genetic disease characterized by clinical and cellular hypersensitivity to ultraviolet radiation and DNA repair defects. Patients with xeroderma pigmentosum experience sun-induced cutaneous and ocular abnormalities, including cancer. Some develop neurological disorders. We describe the case of a 2 year-old child with DeSanctis-Cacchione's syndrome, with severe neurological deterioration associated with schizencephaly. In the current clinical classification of xeroderma pigmentosum, the term is reserved for cases with severe neurological disorders linked to dwarfism and immature sexual development. The association of xeroderma pigmentosum with schizencephaly has not to date been reported in the literature.
着色性干皮病是一种罕见的遗传性疾病,其特征为临床和细胞对紫外线辐射过敏以及DNA修复缺陷。着色性干皮病患者会出现阳光诱发的皮肤和眼部异常,包括癌症。一些患者还会发展为神经障碍。我们描述了一名患有德桑蒂斯 - 卡基奥内综合征的2岁儿童的病例,该患儿伴有与脑裂畸形相关的严重神经功能恶化。在目前着色性干皮病的临床分类中,该术语仅用于与侏儒症和性发育不成熟相关的严重神经障碍病例。迄今为止,文献中尚未报道着色性干皮病与脑裂畸形的关联。