Albinism and Primary Immunodeficiency in Infants: A Case Study of Griscelli Syndrome
Nadia Bouhafs,
Chaimae N'joumi,
Aziza Elouali
et al.
Abstract:Griscelli syndrome (GS) type II is a rare hereditary disorder characterized by partial albinism, immunodeficiency, and the subsequent development of hemophagocytic syndrome (HPS). Herein, we present a case involving a four-month-old infant admitted to our facility due to a prolonged fever complicated by HPS. The diagnosis of GS type 2 was established based on a constellation of clinical and laboratory findings: consanguinity, familial history of early infectious fatalities, ocular-cutaneous hypopigmentation, c… Show more
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