Publication Type : Case Reports
Publisher : Springer
Source : Indian Journal of Otolaryngology and Head & Neck Surgery, 2022
Url : https://link.springer.com/article/10.1007/s12070-021-02599-5
Campus : Faridabad
School : School of Medicine
Year : 2022
Abstract : Neurofibromatosis type 2 (NF2) is a monogenic condition caused by mutations in the NF2 gene. Examination of skin and eyes and parental screening play a key role in the diagnosis of pediatric NF2. We report a four-year-old boy, who presented sub-acutely with unilateral vision loss, ptosis and exotropia with a positive family history of NF2.
Cite this Research Publication : Singanamalla, Bhanudeep, Sameer Vyas, Priyanka Madaan, and Lokesh Saini. "Ptosis, Visual Blurring, and Multiple Cranial Nerve Tumors: Do We Know the Culprit." Indian Journal of Otolaryngology and Head & Neck Surgery 74, no. Suppl 3 (2022): 5361-5363.