A multidisciplinary approach to inherited retinal dystrophies from diagnosis to initial care: a narrative review with inputs from clinical practice

Abstract Background Non-syndromic inherited retinal dystrophies (IRDs) such as retinitis pigmentosa or Leber congenital amaurosis generally manifest between early childhood and late adolescence, imposing profound long-term impacts as a result of vision impairment or blindness. IRDs are highly hetero...

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Váldodahkkit:	Vittoria Murro, Sandro Banfi, Francesco Testa, Giancarlo Iarossi, Benedetto Falsini, Andrea Sodi, Sabrina Signorini, Achille Iolascon, Roberta Russo, Dario Pasquale Mucciolo, Roberto Caputo, Giacomo Maria Bacci, Sara Bargiacchi, Simona Turco, Stefania Fortini, Francesca Simonelli
Materiálatiipa:	Artigo
Giella:	Inglês
Almmustuhtton:	BMC 2023-07-01
Ráidu:	Orphanet Journal of Rare Diseases
Fáttát:	Inherited retinal diseases Visual function Clinical diagnosis Molecular diagnosis Multidisciplinary Early-onset retinal dystrophy
Liŋkkat:	https://doi.org/10.1186/s13023-023-02798-z
Fáddágilkorat:	Lasit fáddágilkoriid Eai fáddágilkorat, Lasit vuosttaš fáddágilkora!