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Information Journal Paper

Title

A Griscelli Syndrome, with Retropharyngeal Abscess, as the First Clinical Manifestation

Pages

  51-55

Abstract

 Griscelli syndrome (GS) is a rare autosomal recessive disorder, which is characterized by albinism with immunodeficiency and usually causes death in early childhood. Accordingly, this syndrome is a primary immune defects presented with a dilution of pigmentations of the skin and hair, recurrent pulmonary and skin infections, neurologic disorders, hypogammaglobulinemia, and variable cellular immunodeficiency. Moreover, in different phenotypes of the syndrome, three mutations have been mentioned. In most of them, GS leads to death in the first decade of life. Herein, we reported a oneyear-old male child with an upper respiratory infection and retropharyngeal abscess as the first clinical manifestation.

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    Cite

    APA: Copy

    SHADANI, SHIVA, Safarirad, Molood, Ramezanzadeh, Reyhaneh, Yousefi, Koroush, & Vosughi motlagh, Ahmad. (2020). A Griscelli Syndrome, with Retropharyngeal Abscess, as the First Clinical Manifestation. IMMUNOLOGY AND GENETICS JOURNA, 3(2), 51-55. SID. https://sid.ir/paper/754771/en

    Vancouver: Copy

    SHADANI SHIVA, Safarirad Molood, Ramezanzadeh Reyhaneh, Yousefi Koroush, Vosughi motlagh Ahmad. A Griscelli Syndrome, with Retropharyngeal Abscess, as the First Clinical Manifestation. IMMUNOLOGY AND GENETICS JOURNA[Internet]. 2020;3(2):51-55. Available from: https://sid.ir/paper/754771/en

    IEEE: Copy

    SHIVA SHADANI, Molood Safarirad, Reyhaneh Ramezanzadeh, Koroush Yousefi, and Ahmad Vosughi motlagh, “A Griscelli Syndrome, with Retropharyngeal Abscess, as the First Clinical Manifestation,” IMMUNOLOGY AND GENETICS JOURNA, vol. 3, no. 2, pp. 51–55, 2020, [Online]. Available: https://sid.ir/paper/754771/en

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