GRISCELLI SYNDROME; A CASE REPORT AND REVIEW OF THE LITERATURE

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SHAMSIAN B.SH.; ARZANIAN M.T.; ALAVI S.; ZAREEIFAR S.

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Journal Paper

Paper Information

Journal: Iranian Journal of Child Neurology Year:2007 | Volume:1 | Issue:3 Page(s): 47-51

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Title

GRISCELLI SYNDROME; A CASE REPORT AND REVIEW OF THE LITERATURE

Author(s)

SHAMSIAN B.SH. | ARZANIAN M.T. | ALAVI S. | ZAREEIFAR S. | Issue Writer Certificate

Keywords

GRISCELLI SYNDROME

HEMOPHAGOCYTOSIS

ALBINISM

Abstract

GRISCELLI SYNDROME (GS) is a rare disease first described in 1978. It is inherited in autosomal recessive pattern. This disease is characterized by partial ALBINISM, pigmentation dilution, cellular immunodeficiency, neurological involvement & uncontrolled phases of macrophage & lymphocyte activation.We report a 5 months Old Iranian girl presenting with silver-gray hair, eyelashes and eyebrows, hepatosplenomegaly, pancytopenia, HEMOPHAGOCYTOSIS and progressive neurologic deterioration. GRISCELLI SYNDROME can be suggested according to her symptoms. The chemotherapy was not effective for her and she died due to multi organ failure.

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APA: Copy

SHAMSIAN, B.SH., ARZANIAN, M.T., ALAVI, S., & ZAREEIFAR, S.. (2007). GRISCELLI SYNDROME; A CASE REPORT AND REVIEW OF THE LITERATURE. IRANIAN JOURNAL OF CHILD NEUROLOGY (IJCN), 1(3), 47-51. SID. https://sid.ir/paper/303179/en

Vancouver: Copy

SHAMSIAN B.SH., ARZANIAN M.T., ALAVI S., ZAREEIFAR S.. GRISCELLI SYNDROME; A CASE REPORT AND REVIEW OF THE LITERATURE. IRANIAN JOURNAL OF CHILD NEUROLOGY (IJCN)[Internet]. 2007;1(3):47-51. Available from: https://sid.ir/paper/303179/en

IEEE: Copy

B.SH. SHAMSIAN, M.T. ARZANIAN, S. ALAVI, and S. ZAREEIFAR, “GRISCELLI SYNDROME; A CASE REPORT AND REVIEW OF THE LITERATURE,” IRANIAN JOURNAL OF CHILD NEUROLOGY (IJCN), vol. 1, no. 3, pp. 47–51, 2007, [Online]. Available: https://sid.ir/paper/303179/en

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