Please use this identifier to cite or link to this item: http://doi.org/10.25358/openscience-8754
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dc.contributor.authorAghayeva, Fidan A.-
dc.contributor.authorSchuster, Alexander K.-
dc.contributor.authorDiel, Heidi-
dc.contributor.authorChronopoulos, Panagiotis-
dc.contributor.authorWagner, Felix M.-
dc.contributor.authorGrehn, Franz-
dc.contributor.authorPirlich, Nina-
dc.contributor.authorSchweiger, Susann-
dc.contributor.authorPfeiffer, Norbert-
dc.contributor.authorHoffmann, Esther M.-
dc.date.accessioned2023-02-03T09:14:09Z-
dc.date.available2023-02-03T09:14:09Z-
dc.date.issued2022-
dc.identifier.urihttps://openscience.ub.uni-mainz.de/handle/20.500.12030/8770-
dc.description.abstractObjective The aim of this prospective pilot study is to establish an initial database to register patients diagnosed with different types of childhood glaucoma and the set-up of a national registry for childhood glaucoma (ReCG) in Germany. 28 children with different types of diagnosed childhood glaucoma, who were admitted and treated at the Childhood Glaucoma Center of the University Medical Center Mainz, Germany were included. Main outcome measures were the type of childhood glaucoma, mean intraocular pressure (IOP) and genetic data of the patients. Results The documents and questionnaires for each individual included: informed consent form of the parents, medical history form of the child, patient’s gestational history questionnaire and general anesthesia examination form. Primary congenital and secondary childhood glaucoma were revealed in 11 (39%) and 17 (61%) patients, respectively. The mean IOP measured with Perkins tonometer in all patients under general anesthesia at the time of inclusion was 17.5 ± 11.8 mmHg in the right and 17 ± 8.9 mmHg in the left eyes. In 33% of children with glaucoma mutations in the CYP1B1, FOXC1, LTBP2 and TEK genes were found. The development of specific questionnaires for childhood glaucoma provides detailed baseline data to establish a ReCG in Germany for the first time.en_GB
dc.description.sponsorshipGefördert durch die Deutsche Forschungsgemeinschaft (DFG) - Projektnummer 491381577de
dc.language.isoengde
dc.rightsCC BY*
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/*
dc.subject.ddc610 Medizinde_DE
dc.subject.ddc610 Medical sciencesen_GB
dc.titleChildhood glaucoma registry in Germany : initial database, clinical care and research (pilot study)en_GB
dc.typeZeitschriftenaufsatzde
dc.identifier.doihttp://doi.org/10.25358/openscience-8754-
jgu.type.contenttypeScientific articlede
jgu.type.dinitypearticleen_GB
jgu.type.versionPublished versionde
jgu.type.resourceTextde
jgu.organisation.departmentFB 04 Medizinde
jgu.organisation.number2700-
jgu.organisation.nameJohannes Gutenberg-Universität Mainz-
jgu.rights.accessrightsopenAccess-
jgu.journal.titleBMC Research Notesde
jgu.journal.volume15de
jgu.pages.alternative32de
jgu.publisher.year2022-
jgu.publisher.nameBMCde
jgu.publisher.placeLondonde
jgu.publisher.issn1756-0500de
jgu.organisation.placeMainz-
jgu.subject.ddccode610de
jgu.publisher.doi10.1186/s13104-022-05921-8de
jgu.organisation.rorhttps://ror.org/023b0x485-
jgu.subject.dfgLebenswissenschaftende
Appears in collections:DFG-491381577-G

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