Neonatal Onset Glaucoma in a Case with Gorlin-Goltz Syndrome: An Unusual Association
To report a unique presentation of Gorlin-Goltz syndrome (GGS) with congenital glaucoma. We report a case of a 3-month-old female patient with bilateral uncontrolled intraocular pressures (IOP), who was already diagnosed with GGS. Examination under anesthesia demonstrated microcornea, iris coloboma,...
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Veröffentlicht in: | Journal of current glaucoma practice 2021-05, Vol.15 (2), p.99-101 |
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description | To report a unique presentation of Gorlin-Goltz syndrome (GGS) with congenital glaucoma.
We report a case of a 3-month-old female patient with bilateral uncontrolled intraocular pressures (IOP), who was already diagnosed with GGS. Examination under anesthesia demonstrated microcornea, iris coloboma, lens subluxation in both eyes, and edematous cornea in the left eye. Intraocular pressure was 17 mm Hg in OD and 35 mm Hg in OS with Icare (Icare® PRO) tonometer on repetitive measurements. On dilated fundus examination, a large chorioretinal coloboma was seen on both eyes.
On physical examination, cutaneous, dental, and skeletal anomalies associated with the GGS were found. As previously reported ocular abnormalities associated with the GGS; coloboma and microphthalmia were noted. In addition, congenital glaucoma which is not one of the known associations of GGS was also detected. For treatment, 270° transscleral diode cyclophotoablation was performed for the left eye and medical treatment was reorganized for both eyes.
Neonatal-onset glaucoma might be one of the important ocular manifestations of GGS.
Tefon Arıbaş AB, Aktaş Z, Özdek Ş. Neonatal Onset Glaucoma in a Case with Gorlin-Goltz Syndrome: An Unusual Association. J Curr Glaucoma Pract 2021;15(2):99-101. |
doi_str_mv | 10.5005/jp-journals-10078-1308 |
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We report a case of a 3-month-old female patient with bilateral uncontrolled intraocular pressures (IOP), who was already diagnosed with GGS. Examination under anesthesia demonstrated microcornea, iris coloboma, lens subluxation in both eyes, and edematous cornea in the left eye. Intraocular pressure was 17 mm Hg in OD and 35 mm Hg in OS with Icare (Icare® PRO) tonometer on repetitive measurements. On dilated fundus examination, a large chorioretinal coloboma was seen on both eyes.
On physical examination, cutaneous, dental, and skeletal anomalies associated with the GGS were found. As previously reported ocular abnormalities associated with the GGS; coloboma and microphthalmia were noted. In addition, congenital glaucoma which is not one of the known associations of GGS was also detected. For treatment, 270° transscleral diode cyclophotoablation was performed for the left eye and medical treatment was reorganized for both eyes.
Neonatal-onset glaucoma might be one of the important ocular manifestations of GGS.
Tefon Arıbaş AB, Aktaş Z, Özdek Ş. Neonatal Onset Glaucoma in a Case with Gorlin-Goltz Syndrome: An Unusual Association. J Curr Glaucoma Pract 2021;15(2):99-101.</description><identifier>ISSN: 0974-0333</identifier><identifier>EISSN: 0975-1947</identifier><identifier>DOI: 10.5005/jp-journals-10078-1308</identifier><identifier>PMID: 34720501</identifier><language>eng</language><publisher>India: Jaypee Brothers Medical Publishers</publisher><subject>Case Report</subject><ispartof>Journal of current glaucoma practice, 2021-05, Vol.15 (2), p.99-101</ispartof><rights>Copyright © 2021; Jaypee Brothers Medical Publishers (P) Ltd.</rights><rights>Copyright © 2021; Jaypee Brothers Medical Publishers (P) Ltd. 2021</rights><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3298-5a1984911c6ef4d6559df499b2aa22a4cfac49f272fbc8380c01ea915f0bd0a23</citedby><cites>FETCH-LOGICAL-c3298-5a1984911c6ef4d6559df499b2aa22a4cfac49f272fbc8380c01ea915f0bd0a23</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8543741/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8543741/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,27923,27924,53790,53792</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34720501$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Tefon Arıbaş, A B</creatorcontrib><creatorcontrib>Aktaş, Zeynep</creatorcontrib><creatorcontrib>Özdek, Şengül</creatorcontrib><title>Neonatal Onset Glaucoma in a Case with Gorlin-Goltz Syndrome: An Unusual Association</title><title>Journal of current glaucoma practice</title><addtitle>J Curr Glaucoma Pract</addtitle><description>To report a unique presentation of Gorlin-Goltz syndrome (GGS) with congenital glaucoma.
We report a case of a 3-month-old female patient with bilateral uncontrolled intraocular pressures (IOP), who was already diagnosed with GGS. Examination under anesthesia demonstrated microcornea, iris coloboma, lens subluxation in both eyes, and edematous cornea in the left eye. Intraocular pressure was 17 mm Hg in OD and 35 mm Hg in OS with Icare (Icare® PRO) tonometer on repetitive measurements. On dilated fundus examination, a large chorioretinal coloboma was seen on both eyes.
On physical examination, cutaneous, dental, and skeletal anomalies associated with the GGS were found. As previously reported ocular abnormalities associated with the GGS; coloboma and microphthalmia were noted. In addition, congenital glaucoma which is not one of the known associations of GGS was also detected. For treatment, 270° transscleral diode cyclophotoablation was performed for the left eye and medical treatment was reorganized for both eyes.
Neonatal-onset glaucoma might be one of the important ocular manifestations of GGS.
Tefon Arıbaş AB, Aktaş Z, Özdek Ş. Neonatal Onset Glaucoma in a Case with Gorlin-Goltz Syndrome: An Unusual Association. J Curr Glaucoma Pract 2021;15(2):99-101.</description><subject>Case Report</subject><issn>0974-0333</issn><issn>0975-1947</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNpVkU9LAzEQxYMoVtSvUHL0Es3f7saDUIpWQfSgnsM0m7Upu0lNdpX66V21igaGBGbem0d-CI0ZPVWUqrPVmqxinwI0mTBKi5IwQcsddEB1oQjTstj9ektChRAjdJzzig5HDqX1PhoJWXCqKDtAj3cuBuigwfchuw7PG-htbAH7gAHPIDv85rslnsfU-EDmsene8cMmVCm27hxPA34Kfe4H_TTnaD10PoYjtFcP2dzx9j5ET1eXj7Nrcns_v5lNb4kVXJdEAdOl1IzZiatlNVFKV7XUesEBOAdpa7BS17zg9cKWoqSWMgeaqZouKgpcHKKLb991v2hdZV3oEjRmnXwLaWMiePO_E_zSPMdXUyopCskGg5OtQYovvcudaX22rmkguNhnw5VmnA8fpYbRyfeoTTHn5OrfNYyaTypmtTY_VMwXFfNJZRCO_4b8lf0wEB-ZbYy-</recordid><startdate>20210501</startdate><enddate>20210501</enddate><creator>Tefon Arıbaş, A B</creator><creator>Aktaş, Zeynep</creator><creator>Özdek, Şengül</creator><general>Jaypee Brothers Medical Publishers</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20210501</creationdate><title>Neonatal Onset Glaucoma in a Case with Gorlin-Goltz Syndrome: An Unusual Association</title><author>Tefon Arıbaş, A B ; Aktaş, Zeynep ; Özdek, Şengül</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3298-5a1984911c6ef4d6559df499b2aa22a4cfac49f272fbc8380c01ea915f0bd0a23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Case Report</topic><toplevel>online_resources</toplevel><creatorcontrib>Tefon Arıbaş, A B</creatorcontrib><creatorcontrib>Aktaş, Zeynep</creatorcontrib><creatorcontrib>Özdek, Şengül</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of current glaucoma practice</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Tefon Arıbaş, A B</au><au>Aktaş, Zeynep</au><au>Özdek, Şengül</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Neonatal Onset Glaucoma in a Case with Gorlin-Goltz Syndrome: An Unusual Association</atitle><jtitle>Journal of current glaucoma practice</jtitle><addtitle>J Curr Glaucoma Pract</addtitle><date>2021-05-01</date><risdate>2021</risdate><volume>15</volume><issue>2</issue><spage>99</spage><epage>101</epage><pages>99-101</pages><issn>0974-0333</issn><eissn>0975-1947</eissn><abstract>To report a unique presentation of Gorlin-Goltz syndrome (GGS) with congenital glaucoma.
We report a case of a 3-month-old female patient with bilateral uncontrolled intraocular pressures (IOP), who was already diagnosed with GGS. Examination under anesthesia demonstrated microcornea, iris coloboma, lens subluxation in both eyes, and edematous cornea in the left eye. Intraocular pressure was 17 mm Hg in OD and 35 mm Hg in OS with Icare (Icare® PRO) tonometer on repetitive measurements. On dilated fundus examination, a large chorioretinal coloboma was seen on both eyes.
On physical examination, cutaneous, dental, and skeletal anomalies associated with the GGS were found. As previously reported ocular abnormalities associated with the GGS; coloboma and microphthalmia were noted. In addition, congenital glaucoma which is not one of the known associations of GGS was also detected. For treatment, 270° transscleral diode cyclophotoablation was performed for the left eye and medical treatment was reorganized for both eyes.
Neonatal-onset glaucoma might be one of the important ocular manifestations of GGS.
Tefon Arıbaş AB, Aktaş Z, Özdek Ş. Neonatal Onset Glaucoma in a Case with Gorlin-Goltz Syndrome: An Unusual Association. J Curr Glaucoma Pract 2021;15(2):99-101.</abstract><cop>India</cop><pub>Jaypee Brothers Medical Publishers</pub><pmid>34720501</pmid><doi>10.5005/jp-journals-10078-1308</doi><tpages>3</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Case Report |
title | Neonatal Onset Glaucoma in a Case with Gorlin-Goltz Syndrome: An Unusual Association |
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