• JAAPA · Apr 2015

    Case Reports

    A rare cause of hearing loss in a child.

    • Michelle Musallam and Gina Quon.
    • Michelle Musallam and Gina Quon practice otolaryngology at Children's Medical Center in Dallas, Tex. The authors have disclosed no potential conflicts of interest, financial or otherwise.
    • JAAPA. 2015 Apr 1; 28 (4): 32-7.

    AbstractNeurofibromatosis type 2 is a rare genetic disease affecting the central and peripheral nervous systems and characterized by schwannomas, meningiomas, and ependymomas. Prompt symptom recognition, diagnosis, and proper referrals can increase treatment effectiveness and decrease the mortality risk of this life-threatening disease.

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