| Identifier |
91_12 |
| Title |
Ocular Manifestations of Congenital/Inherited Diseases |
| Creator |
William Fletcher Hoyt, MD |
| Affiliation |
UCSF Medical Center |
| Contributing Institution |
AAO/NANOS - American Academy of Ophthalmology / North American Neuro-Ophthalmology Society |
| Subject |
Neurofibromatosis, Type 1 |
| Description |
Neurofibromatosis, type 1, is an autosomal dominant phakomatosis characterized by Lisch nodules of the iris (hamartomas) plexiform neurofibromas, café-au-lait spots on the skin, and axillary freckling. Intracranial tumors such as optic pathway gliomas may occur. Disease/Diagnosis: Neurofibromatosis, Type 1. |
| Date |
1999 |
| Date Digital |
2004 |
| Language |
eng |
| Format |
image/jpeg |
| Type |
Image |
| Source |
AAO/NANOS Clinical neuro-ophthalmology : image collection for ophthalmic practitioners. American Academy of Ophthalmology [electronic resource], [San Francisco, Calif.] : AAO, c1999. |
| Relation is Part of |
Case 26 |
| Collection |
Neuro-Ophthalmology Virtual Education Library: NOVEL http://NOVEL.utah.edu |
| Publisher |
North American Neuro-Ophthalmology Society |
| Holding Institution |
Spencer S. Eccles Health Sciences Library, University of Utah, 10 N 1900 E SLC, UT 84112-5890 |
| Rights Management |
Copyright 1999. For further information regarding the rights to this collection, please visit: https://NOVEL.utah.edu/about/copyright |
| ARK |
ark:/87278/s6865g2n |
| Setname |
ehsl_novel_aao_nanos |
| ID |
176717 |
| Reference URL |
https://collections.lib.utah.edu/ark:/87278/s6865g2n |
