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Retina Case: “External Pallor”

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Presentation on theme: "Retina Case: “External Pallor”"— Presentation transcript:

1 Retina Case: “External Pallor”
Kevin Lowder, MD – PGY3 03/01/2019

2 Patient Presentation CC HPI Difficulty driving at night
21 yo WF with hx of mild nystagmus OU, p/w difficulty driving at night and light sensitivity. Pt was referred to retina by outside ophthalmology practice for suspected retinal dystrophy given abnormal exam and OCT findings.

3 History (Hx) Past Ocular Hx: Nystagmus OU Ocular Meds: none
PMH: Migraines, HTN, IBS, Anxiety Fam Hx: Non-contributory Meds: Linaclotide, Zonisamide, birth control Allergies: NKDA Social Hx: Never smoker, no EtOH or drugs RoS: Negative Linaclotide = for IBS Zonisamide = anti-convulsant 3

4 Physical Exam OD OS BCVA 20/30 20/50+2 Pupils 4mm. Round. Brisk.
No rAPD IOP 14 mmHg 15 mmHg EOM full CVF Adnexa Small amplitude nystagmus

5

6 Physical Exam SLE OD OS External/Lids WNL Conj/Sclera White, Quiet
Cornea Epithelium intact Ant Chamber Normal depth, Quiet Iris subtle transillumination defects Lens clear

7 Posterior Exam (Fundus Photos)

8 OCT Macula: Foveal Hypoplasia OU
Foveal cut OD Foveal cut OS

9 Assessment 21 yo WF with ocular albinism Albinoid external appearance
Light sensitivity Nystagmus Foveal hypoplasia Iris transillumination defects Suboptimal BCVA

10 Other Features: Abnormal decussation of the visual pathways
Normal ~53%; in ocular albinism can be 90% Strabismus/loss of stereopsis  related to abnormal decussation Can be tested with VEP Photophobia Refractive errors (myopia, hyperopia, astigmatism) Poor vision (ranging from mild to < 20/200)

11 Main Subsets of Albinism
Oculocutaneous: AR inheritance Tyrosine-positive: gradually accumulate more pigment Tyrosine-negative: do not Chédiak-Higashi syndrome: neutropenia/blood disorder that leads to deadly infections and bleeding Hermansky-Pudlak syndrome: platelet defect that causes easy bruising and bleeding (3 P’s: Pigment-less, Platelets, Puerto Ricans) Ocular albinism: X-linked (most common) True albinism: fovea is hypoplastic, BCVA is decreased Albinoidism: (AD) foveal pit is present, VA normal, no nystagmus Albinoidism = AD with incomplete penetrance

12 Treatment/Plan Observe/treat symptoms Consider genetics consult
Hematology consult if any suspicion for blood disorders

13 References Kim, JM. (2014, December). Albinism. Retrieved from Basic Clinical Sciences Course, Section 12: Retina and Vitreous. American Academy of Ophthalmology, Pages 247-8


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