مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

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Information Journal Paper

Title

FIRST REPORT OF GRISCELLI SYNDROME FROM AFGHAN POPULATION IN IRAN

Pages

  38-40

Abstract

 A 4 month old Afghan male infant presented with PARTIAL ALBINISM, hepatosplenomegaly and pancytopenia. Skin and hair shaft microscopic examination revealed large clumped melanosomes and GRISCELLI SYNDROME was diagnosed. Unless treated with bone marrow transplantation, it is a fatal disease in accelerated phase. Pediatricians should consider this syndrome in infants with abnormal light hair because early diagnosis could be life saving.

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  • Cite

    APA: Copy

    SAYAH FAR, SH., KARIMI, A., FAHIMZAD, S.A.R., GHOROUBI, J., GHARIB, A., & ARMIN, SH.. (2008). FIRST REPORT OF GRISCELLI SYNDROME FROM AFGHAN POPULATION IN IRAN. JOURNAL OF RESEARCH IN MEDICAL SCIENCES (JRMS), 13(1), 38-40. SID. https://sid.ir/paper/551145/en

    Vancouver: Copy

    SAYAH FAR SH., KARIMI A., FAHIMZAD S.A.R., GHOROUBI J., GHARIB A., ARMIN SH.. FIRST REPORT OF GRISCELLI SYNDROME FROM AFGHAN POPULATION IN IRAN. JOURNAL OF RESEARCH IN MEDICAL SCIENCES (JRMS)[Internet]. 2008;13(1):38-40. Available from: https://sid.ir/paper/551145/en

    IEEE: Copy

    SH. SAYAH FAR, A. KARIMI, S.A.R. FAHIMZAD, J. GHOROUBI, A. GHARIB, and SH. ARMIN, “FIRST REPORT OF GRISCELLI SYNDROME FROM AFGHAN POPULATION IN IRAN,” JOURNAL OF RESEARCH IN MEDICAL SCIENCES (JRMS), vol. 13, no. 1, pp. 38–40, 2008, [Online]. Available: https://sid.ir/paper/551145/en

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