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
| Title | Creator | Description | ||
|---|---|---|---|---|
| 351 |
 |
Ocular Manifestations of Systemic Disorders | Rosa A. Tang, MD | Thyroid eye disease may cause proptosis and extraocular muscle enlargement that may be seen on orbital imaging studies. In general, coronal images allow the best visualization of the extraocular muscle enlargement. Pair with 94_45 and 94_46. |
| 352 |
 |
Ocular Manifestations of Systemic Disorders | Rosa A. Tang, MD | Thyroid eye disease can result in significant upper eyelid retraction and axial proptosis resulting in exposure keratopathy. |
| 353 |
 |
Optic Neuropathies | Michael Wall, MD | Optic disc edema with a macular star figure may occur in infectious diseases (eg, cat-scratch disease, syphilis, tuberculosis, Lyme disease), inflammatory diseases (eg, sarcoid), ischemic diseases (anterior ischemic optic neuropathy), and in papilledema. Infectious causes should be sought in patient... |
| 354 |
 |
Systemic Disorders With Optic Nerve and Retinal Findings | Joel M. Weinstein, MD | This 46-year-old woman noted progressive bilateral visual loss over a 10-month period. She had a malignant melanoma removed from her right thigh 2 years ago and excisional biopsy of an inguinal node metastasis 8 months ago. She also complained of poor night vision and rare intermittent ""sparkles"" ... |
| 355 |
 |
Systemic Disorders With Optic Nerve and Retinal Findings | Joel M. Weinstein, MD | This 46-year-old woman noted progressive bilateral visual loss over a 10-month period. She had a malignant melanoma removed from her right thigh 2 years ago and excisional biopsy of an inguinal node metastasis 8 months ago. She also complained of poor night vision and rare intermittent ""sparkles"" ... |
| 356 |
 |
Systemic Disorders With Optic Nerve and Retinal Findings | Joel M. Weinstein, MD | This 46-year-old woman noted progressive bilateral visual loss over a 10-month period. She had a malignant melanoma removed from her right thigh 2 years ago and excisional biopsy of an inguinal node metastasis 8 months ago. She also complained of poor night vision and rare intermittent ""sparkles"" ... |
| 357 |
 |
Systemic Disorders With Optic Nerve and Retinal Findings | Joel M. Weinstein, MD | This 46-year-old woman noted progressive bilateral visual loss over a 10-month period. She had a malignant melanoma removed from her right thigh 2 years ago and excisional biopsy of an inguinal node metastasis 8 months ago. She also complained of poor night vision and rare intermittent ""sparkles"" ... |
| 358 |
 |
Isolated Congenital Optic Disc Anomalies | William Fletcher Hoyt, MD | 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. |
| 359 |
 |
Isolated Congenital Optic Disc Anomalies | William Fletcher Hoyt, MD | 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. |
| 360 |
 |
Isolated Congenital Optic Disc Anomalies | William Fletcher Hoyt, MD | 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. |
| 361 |
 |
Ocular Manifestations of Congenital/Inherited Diseases | William Fletcher Hoyt, MD | 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. |