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Pigmentary glaucoma accompanied by Usher syndrome.
J Glaucoma. 2012 Aug; 21(6):392-3.JG

Abstract

PURPOSE

To report a case of pigmentary glaucoma (PG) accompanied by Usher syndrome.

DESIGN

Case report.

METHODS

The results were presented after standard ocular examination, visual field test, anterior segment and fundus photography, electroretinography, and otolaryngology consultation were conducted.

RESULTS

Typical retinitis pigmentosa, flat electroretinography, congenital sensorineural hearing loss, high intraocular pressure, Krukenberg spindle, iris concavity, radial iris transillumination defect, severe pigment deposition on the trabecular meshwork, and glaucomatous optic nerve damage were indicative of PG accompanied by Usher syndrome.

CONCLUSIONS

In some rare cases, PG may coexist with Usher syndrome. Common findings of Usher syndrome, including night blindness, impaired vision, visual field defects, and retinal changes may distract the clinician from considering the diagnosis of glaucoma. Such association should be borne in mind to make a timely diagnosis and treatment possible.

Authors+Show Affiliations

Noor Ophthalmology Research Center, Noor Eye Hospital, Tehran, Iran. bkouchaki@noorvision.comNo affiliation info available

Pub Type(s)

Case Reports
Journal Article

Language

eng

PubMed ID

21467951

Citation

Koucheki, Behrooz, and Kamran Hodjat Jalali. "Pigmentary Glaucoma Accompanied By Usher Syndrome." Journal of Glaucoma, vol. 21, no. 6, 2012, pp. 392-3.
Koucheki B, Jalali KH. Pigmentary glaucoma accompanied by Usher syndrome. J Glaucoma. 2012;21(6):392-3.
Koucheki, B., & Jalali, K. H. (2012). Pigmentary glaucoma accompanied by Usher syndrome. Journal of Glaucoma, 21(6), 392-3. https://doi.org/10.1097/IJG.0b013e3182127ac5
Koucheki B, Jalali KH. Pigmentary Glaucoma Accompanied By Usher Syndrome. J Glaucoma. 2012;21(6):392-3. PubMed PMID: 21467951.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Pigmentary glaucoma accompanied by Usher syndrome. AU - Koucheki,Behrooz, AU - Jalali,Kamran Hodjat, PY - 2011/4/7/entrez PY - 2011/4/7/pubmed PY - 2012/11/3/medline SP - 392 EP - 3 JF - Journal of glaucoma JO - J Glaucoma VL - 21 IS - 6 N2 - PURPOSE: To report a case of pigmentary glaucoma (PG) accompanied by Usher syndrome. DESIGN: Case report. METHODS: The results were presented after standard ocular examination, visual field test, anterior segment and fundus photography, electroretinography, and otolaryngology consultation were conducted. RESULTS: Typical retinitis pigmentosa, flat electroretinography, congenital sensorineural hearing loss, high intraocular pressure, Krukenberg spindle, iris concavity, radial iris transillumination defect, severe pigment deposition on the trabecular meshwork, and glaucomatous optic nerve damage were indicative of PG accompanied by Usher syndrome. CONCLUSIONS: In some rare cases, PG may coexist with Usher syndrome. Common findings of Usher syndrome, including night blindness, impaired vision, visual field defects, and retinal changes may distract the clinician from considering the diagnosis of glaucoma. Such association should be borne in mind to make a timely diagnosis and treatment possible. SN - 1536-481X UR - https://www.unboundmedicine.com/medline/citation/21467951/Pigmentary_glaucoma_accompanied_by_Usher_syndrome_ DB - PRIME DP - Unbound Medicine ER -