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Griscelli Syndrome Type 3: Two New Cases and Review of the Literature

机译:Griscelli综合征类型3:两个新病例和文献复习

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摘要

A 3-year-old Arab boy with a history of hypoplastic left heart syndrome was referred to the pediatric dermatology clinic at Sheba Medical Center for evaluation of hypomelanosis, manifested by fair skin pigmentation and silvery-grey hair, eyebrows, and eyelashes. The child had one older brother with similar hypopigmentation and another older brother who had died of congenital heart disease. The child had no history of neurologic deficits or immunodeficiency and no additional findings on clinical evaluation.
机译:一名3岁的患有左心发育不全综合征史的阿拉伯男孩被转到Sheba医学中心的儿科皮肤病诊所评估黑素沉着病,表现为皮肤色素沉着,银灰色的头发,眉毛和睫毛。这个孩子有一个色素沉着相似的哥哥和另一个死于先天性心脏病的哥哥。这名儿童没有神经系统缺陷或免疫缺陷的病史,并且在临床评估中没有其他发现。

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