author = {Nandi, Sunanda. and Kuli, Jawahar.}, title = {{A woman with oculocutaneous manifestation of neurofibromatosis type 1: A rare case report}}, journal ={International Journal of Health & Allied Sciences}, volume ={10}, number ={1}, pages = {83-86}, doi = {10.4103/ijhas.IJHAS_82_20}, year = {2021}, abstract ={ Neurofibromatosis type 1 (NF-1) is an autosomal dominant disorder involving multiple systems and affects approximately 1 out of 3000 persons. Ocular manifestations are very rare with Lisch nodules, plexiform neurofibroma, and optic pathway gliomas. The proper diagnosis of NF-1 is a crucial task for a clinician due to the various clinical manifestations including vision and life-threatening malignancies in few patients, which may arise in the different phases of life. Here, we present the case of a 45-year-old woman with NF-1 presenting with rare ocular features along with systemic manifestation of the disease. }, URL ={https://www.ijhas.in/article.asp?issn=2278-344X;year=2021;volume=10;issue=1;spage=83;epage=86;aulast=Nandi;t=6}, eprint ={https://www.ijhas.in/article.asp?issn=2278-344X;year=2021;volume=10;issue=1;spage=83;epage=86;aulast=Nandi;t=6} }