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Griscelli Syndrome Type 3: Two New Cases and Review of the Literature
Authors:Ariella Nouriel M.D.  Jonah Zisquit M.D.  Alexander M. Helfand M.D.  Shoshana Greenberger M.D.   Ph.D.
Affiliation:Department of Dermatology, Sheba Medical Center, Tel Hashomer, Ramat Gan, Israel
Abstract: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.
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