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Updated: Apr 15, 2026

Intrathecal Application of a Fluorescent Dye for the Identification of Cerebrospinal Fluid Leaks in Cochlear Malformation
Published on: February 29, 2020
A rare cause of hearing loss in a child
1Michelle 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.
Abstract:
Neurofibromatosis 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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