Ipsilateral facial and uveal arteriovenous and capillary angioma, microphthalmos, heterochromia of the iris, and hypotony: an oculocutaneous syndrome simulating Sturge-Weber syndrome.
Publication
, Conference
Gass, JD
Published in: Trans Am Ophthalmol Soc
1996
Sturge-Weber syndrome is a disorder characterized by ipsilateral cavernous hemangioma of the face, uvea, and brain in patients who may present with an enlarged eye, exudative retinal detachment, glaucoma, and seizures. This report presents the clinicopathologic findings of an otherwise healthy infant with ipsilateral arteriovenous and capillary hemangiomas of the face and uveal tract, microphthalmos, iris heterochromia, hypotony, and absence of central nervous system involvement. The association of an arteriovenous-capillary angioma of the ocular adnexa and ipsilateral uveal tract is a syndrome that is distinct from Sturge-Weber syndrome.
Duke Scholars
Published In
Trans Am Ophthalmol Soc
ISSN
0065-9533
Publication Date
1996
Volume
94
Start / End Page
227 / 237
Location
United States
Related Subject Headings
- Uveal Neoplasms
- Uvea
- Sturge-Weber Syndrome
- Retinal Vessels
- Ophthalmology & Optometry
- Ocular Hypotension
- Microphthalmos
- Iris Diseases
- Infant
- Humans
Citation
APA
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ICMJE
MLA
NLM
Gass, J. D. (1996). Ipsilateral facial and uveal arteriovenous and capillary angioma, microphthalmos, heterochromia of the iris, and hypotony: an oculocutaneous syndrome simulating Sturge-Weber syndrome. In Trans Am Ophthalmol Soc (Vol. 94, pp. 227–237). United States.
Gass, J. D. “Ipsilateral facial and uveal arteriovenous and capillary angioma, microphthalmos, heterochromia of the iris, and hypotony: an oculocutaneous syndrome simulating Sturge-Weber syndrome.” In Trans Am Ophthalmol Soc, 94:227–37, 1996.
Gass JD. Ipsilateral facial and uveal arteriovenous and capillary angioma, microphthalmos, heterochromia of the iris, and hypotony: an oculocutaneous syndrome simulating Sturge-Weber syndrome. In: Trans Am Ophthalmol Soc. 1996. p. 227–37.
Gass, J. D. “Ipsilateral facial and uveal arteriovenous and capillary angioma, microphthalmos, heterochromia of the iris, and hypotony: an oculocutaneous syndrome simulating Sturge-Weber syndrome.” Trans Am Ophthalmol Soc, vol. 94, 1996, pp. 227–37.
Gass JD. Ipsilateral facial and uveal arteriovenous and capillary angioma, microphthalmos, heterochromia of the iris, and hypotony: an oculocutaneous syndrome simulating Sturge-Weber syndrome. Trans Am Ophthalmol Soc. 1996. p. 227–237.
Published In
Trans Am Ophthalmol Soc
ISSN
0065-9533
Publication Date
1996
Volume
94
Start / End Page
227 / 237
Location
United States
Related Subject Headings
- Uveal Neoplasms
- Uvea
- Sturge-Weber Syndrome
- Retinal Vessels
- Ophthalmology & Optometry
- Ocular Hypotension
- Microphthalmos
- Iris Diseases
- Infant
- Humans