The Ocular Phenotype in Primary Hyperoxaluria Type 1

To investigate ophthalmic features in a large group of patients with primary hyperoxaluria type 1 (PH1) and to determine the relation between ocular involvement and systemic disease severity. Retrospective, cross-sectional, multicenter study of the OxalEurope Registry Network. Sixty-eight patients w...

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Veröffentlicht in:	American journal of ophthalmology 2019-10, Vol.206, p.184-191
Hauptverfasser:	Birtel, Johannes, Herrmann, Philipp, Garrelfs, Sander F., Dulz, Simon, Atiskova, Yevgeniya, Diederen, Roselie M., Gliem, Martin, Brinkert, Florian, Holz, Frank G., Boon, Camiel J.F., Hoppe, Bernd, Charbel Issa, Peter
Format:	Artikel
Sprache:	eng
Schlagworte:	Adolescent Adult Age Biomarkers Child Child, Preschool Cross-Sectional Studies Disease Progression Family medical history Female Fluorescein Angiography - methods Fundus Oculi Genotype & phenotype Humans Hyperoxaluria, Primary - complications Hyperoxaluria, Primary - diagnosis Hyperoxaluria, Primary - metabolism Infant Infant, Newborn Kidneys Liver Male Middle Aged Oxalates - metabolism Patients Phenotype Plasma Retina - metabolism Retina - pathology Retinal Diseases - diagnosis Retinal Diseases - etiology Retinal Diseases - metabolism Retrospective Studies Standard deviation Statistical analysis Systemic diseases Tomography, Optical Coherence - methods Variance analysis Visual Acuity Young Adult
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