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Nat Med ; 25(2): 225-228, 2019 02.
Article in English | MEDLINE | ID: mdl-30559420

ABSTRACT

Photoreceptor ciliopathies constitute the most common molecular mechanism of the childhood blindness Leber congenital amaurosis. Ten patients with Leber congenital amaurosis carrying the c.2991+1655A>G allele in the ciliopathy gene centrosomal protein 290 (CEP290) were treated (ClinicalTrials.gov no. NCT03140969 ) with intravitreal injections of an antisense oligonucleotide to restore correct splicing. There were no serious adverse events, and vision improved at 3 months. The visual acuity of one exceptional responder improved from light perception to 20/400.


Subject(s)
Cilia/pathology , Leber Congenital Amaurosis/drug therapy , Leber Congenital Amaurosis/physiopathology , Oligonucleotides, Antisense/administration & dosage , Oligonucleotides, Antisense/therapeutic use , Photoreceptor Cells, Vertebrate/pathology , Vision, Ocular , Adult , Alleles , Antigens, Neoplasm/genetics , Cell Cycle Proteins , Cilia/drug effects , Cytoskeletal Proteins , Female , Humans , Intravitreal Injections , Male , Neoplasm Proteins/genetics , Young Adult
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