Avtor/Urednik		Sergouniotis, Panagiotis I.
Naslov		Inherited retinal disorders
Tip		članek
Vol. in št.		Letnik 242, št. 4
Leto izdaje		2019
Obseg		str. 187-194
ISSN		0030-3755 - Ophthalmologica. Journal international d'ophtalmologie. International journal of ophthalmology. Zeitschrift für Augenheilkunde
Jezik		eng
Abstrakt		Incremental advances in the field of retinal genetics have transformed our understanding of inherited retinal disorders and have led to the development of powerful diagnostic tests and promising gene-based therapies. Despite this, successful integration of these developments into routine healthcare is frequently ineffective. Providing robust evidence of benefit can accelerate the implementation of clinical genetic interventions. For example, the adoption of a genetic test is much more likely when the test's clinical utility (i.e. its ability to influence management and health outcomes) has been clearly demonstrated. However, accruing such evidence for rare conditions like inherited retinal disorders is challenging. Conducting sufficiently powered studies requires both efficient study designs and large-scale, international collaboration. Reaching all populations and as many affected individuals as possible is key. Equally important are efforts to precisely and consistently capture phenotypic information, including natural history data. This article summarizes some of the current obstacles to implemen-tation and discusses approaches to overcome these barriers.
Proste vsebinske oznake		redke očesne bolezni podedovana bolezen mrežnice genomska medicina rare eye disease inherited retinal disease genomic medicine