AAO-NANOS Neuro-Ophthalmology Clinical Collection: Derived from the AAO-NANOS Clinical Neuro-Ophthalmology collection produced on CD. The images are of selected cases from the NANOS teaching slide exchange, and the CD was produced under the direction of Larry Frohman, MD and Andrew Lee, MD.
The American Academy of Ophthalmology (AAO); The North American Neuro-Ophthalmology Association (NANOS).
NOVEL: https://novel.utah.edu/
TO
Filters: Collection: ehsl_novel_aao_nanos
| Title | Description | Subject | ||
|---|---|---|---|---|
| 351 |
 |
Ocular Manifestations of Congenital/Inherited Diseases | Tuberous sclerosis is an autosomal dominant phakomatosis characterized by astrocytic hamartomas of the retina or optic nerve, adenoma sebaceum of the face, periungual fibromas, and astrocytic hamartomas of the brain, with secondary seizures and mental retardation. Disease/Diagnosis: Tuberous Scleros... | Tuberous Sclerosis |
| 352 |
 |
Isolated Congenital Optic Disc Anomalies | This patient demonstrates bilateral tilted optic discs. Patients with this congenital optic disc anomaly may be asymptomatic or have bitemporal visual field defects that do not respect the vertical midline. Disease/Diagnosis: Tilted Discs. | Tilted Disc |
| 353 |
 |
Isolated Congenital Optic Disc Anomalies | This patient demonstrates bilateral tilted optic discs. Patients with this congenital optic disc anomaly may be asymptomatic or have bitemporal visual field defects that do not respect the vertical midline. Disease/Diagnosis: Tilted Discs. | Tilted Disc |
| 354 |
 |
Isolated Congenital Optic Disc Anomalies | This patient demonstrates bilateral tilted optic discs. Patients with this congenital optic disc anomaly may be asymptomatic or have bitemporal visual field defects that do not respect the vertical midline. Disease/Diagnosis: Tilted Discs. | Tilted Disc |
| 355 |
|
Isolated Congenital Optic Disc Anomalies | This patient demonstrates bilateral tilted optic discs. Patients with this congenital optic disc anomaly may be asymptomatic or have bitemporal visual field defects that do not respect the vertical midline. Disease/Diagnosis: Tilted Discs. | Tilted Disc |
| 356 |
 |
Ocular Manifestations of Congenital/Inherited Diseases | Image shows a patient with the Laurence-Moon-Biedl syndrome, an autosomal recessive syndrome characterized by obesity, mental retardation, retinitis pigmentosa (see Image 91_07), polydactyly, and hypogonadism. Pair with 91_07. | Laurence-Moon-Biedl Syndrome; Hypertelorism |
| 357 |
 |
Ocular Disease With Retinal Findings | Choroidal folds may result from choroidal tumors, compression on the eye wall from thyroid ophthalmopathy, orbital pseudotumor, orbital tumor, posterior scleritis, hypotony, scleral laceration, retinal detachment, marked hyperopia, or secondary to papilledema. Intraocular pressure measurements, refr... | Acquired Hyperopia |
| 358 |
|
Isolated Congenital Optic Disc Anomalies | This patient demonstrates bilateral tilted optic discs. Patients with this congenital optic disc anomaly may be asymptomatic or have bitemporal visual field defects that do not respect the vertical midline. Disease/Diagnosis: Tilted Discs. | Tilted Disc |
| 359 |
 |
Ocular Manifestations of Congenital/Inherited Diseases | Image shows a patient with the Laurence-Moon_Biedl syndrome, an autosomal recessive syndrome characterized by obesity, mental retardation, retinitis pigmentosa, polydactyly, and hypogonadism. Pair with 91_06. | Laurence-Moon-Biedl Syndrome; Bardet-Biedl Syndrome; Retinitis Pigmentosa |
| 360 |
|
Isolated Congenital Optic Disc Anomalies | This patient demonstrates bilateral tilted optic discs. Patients with this congenital optic disc anomaly may be asymptomatic or have bitemporal visual field defects that do not respect the vertical midline. Disease/Diagnosis: Tilted Discs. | Tilted Disc |
| 361 |
 |
Ocular Manifestations of Congenital/Inherited Diseases | 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... | Neurofibromatosis, Type 1 |
| 362 |
 |
Ocular Manifestations of Congenital/Inherited Diseases | Tuberous sclerosis is an autosomal dominant phakomatosis characterized by astrocytic hamartomas of the retina or optic nerve, adenoma sebaceum of the face, periungual fibromas, and astrocytic hamartomas of the brain, with secondary seizures and mental retardation. Disease/Diagnosis: Tuberous Scleros... | Tuberous Sclerosis |