Congenital glaucoma associated with high hyperopia, an ophthalmic phenotypical manifestation for GLIS3 deletion: case report and review of literature.
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| Title: | Congenital glaucoma associated with high hyperopia, an ophthalmic phenotypical manifestation for GLIS3 deletion: case report and review of literature. |
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| Authors: | Almhmoudi F; Ophthalmology Department, King Fahd Armed Forces Hospital, Jeddah, Saudi Arabia., Abudawood G; Ophthalmology Department, King Fahd Armed Forces Hospital, Jeddah, Saudi Arabia., Khan AO; Ophthalmology Department, Cleveland Clinic, Abu Dhabi, UAE., Dallol A; Noor Diagnostics and Discovery, King Abdullah University of Science and Technology, Thuwal, Saudi Arabia., Almontashiri N; College of Applied Medical Sciences and Center for Genetics and Inherited Diseases, Taibah University, Madinah, Kingdom of Saudi Arabia.; Research Department, King Khaled Eye Specialist Hospital, Riyadh, Saudi Arabia., Alhashem A; Pediatric Genetics Department, Prince Sultan Military Medical City, Riyadh, Saudi Arabia. |
| Source: | Ophthalmic genetics [Ophthalmic Genet] 2025 Dec; Vol. 46 (6), pp. 646-657. Date of Electronic Publication: 2025 Jun 29. |
| Publication Type: | Journal Article; Case Reports; Review; Research Support, Non-U.S. Gov't |
| Journal Info: | Publisher: Informa Healthcare Country of Publication: England NLM ID: 9436057 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1744-5094 (Electronic) Linking ISSN: 13816810 NLM ISO Abbreviation: Ophthalmic Genet Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
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| FullText | Links: – Type: pdflink Text: Availability: 1 |
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| Header | DbId: mdl DbLabel: MEDLINE Ultimate An: 40583116 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Congenital glaucoma associated with high hyperopia, an ophthalmic phenotypical manifestation for GLIS3 deletion: case report and review of literature. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AU" term="%22Almhmoudi+F%22">Almhmoudi F</searchLink>; Ophthalmology Department, King Fahd Armed Forces Hospital, Jeddah, Saudi Arabia.<br /><searchLink fieldCode="AU" term="%22Abudawood+G%22">Abudawood G</searchLink>; Ophthalmology Department, King Fahd Armed Forces Hospital, Jeddah, Saudi Arabia.<br /><searchLink fieldCode="AU" term="%22Khan+AO%22">Khan AO</searchLink>; Ophthalmology Department, Cleveland Clinic, Abu Dhabi, UAE.<br /><searchLink fieldCode="AU" term="%22Dallol+A%22">Dallol A</searchLink>; Noor Diagnostics and Discovery, King Abdullah University of Science and Technology, Thuwal, Saudi Arabia.<br /><searchLink fieldCode="AU" term="%22Almontashiri+N%22">Almontashiri N</searchLink>; College of Applied Medical Sciences and Center for Genetics and Inherited Diseases, Taibah University, Madinah, Kingdom of Saudi Arabia.; Research Department, King Khaled Eye Specialist Hospital, Riyadh, Saudi Arabia.<br /><searchLink fieldCode="AU" term="%22Alhashem+A%22">Alhashem A</searchLink>; Pediatric Genetics Department, Prince Sultan Military Medical City, Riyadh, Saudi Arabia. – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%229436057%22">Ophthalmic genetics</searchLink> [Ophthalmic Genet] 2025 Dec; Vol. 46 (6), pp. 646-657. <i>Date of Electronic Publication: </i>2025 Jun 29. – Name: TypePub Label: Publication Type Group: TypPub Data: Journal Article; Case Reports; Review; Research Support, Non-U.S. Gov't – Name: TitleSource Label: Journal Info Group: Src Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Informa+Healthcare%22">Informa Healthcare </searchLink><i>Country of Publication: </i>England <i>NLM ID: </i>9436057 <i>Publication Model: </i>Print-Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>1744-5094 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2213816810%22">13816810 </searchLink><i>NLM ISO Abbreviation: </i>Ophthalmic Genet <i>Subsets: </i>MEDLINE |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=40583116 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1080/13816810.2025.2514526 Languages: – Code: eng Text: English PhysicalDescription: Pagination: StartPage: 646 Titles: – TitleFull: Congenital glaucoma associated with high hyperopia, an ophthalmic phenotypical manifestation for GLIS3 deletion: case report and review of literature. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Almhmoudi F – PersonEntity: Name: NameFull: Abudawood G – PersonEntity: Name: NameFull: Khan AO – PersonEntity: Name: NameFull: Dallol A – PersonEntity: Name: NameFull: Almontashiri N – PersonEntity: Name: NameFull: Alhashem A IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 12 Text: 2025 Dec Type: published Y: 2025 Identifiers: – Type: issn-electronic Value: 1744-5094 Numbering: – Type: volume Value: 46 – Type: issue Value: 6 Titles: – TitleFull: Ophthalmic genetics Type: main |
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