Klinische Monatsblatter fur Augenheilkunde · 2018
[Ciliopathies].
СтатьяОбзорНазвание и аннотация: Перевод в очереди
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Gerth-Kahlert Christina, Koller Samuel
Аннотация
Ciliopathies are disorders caused by ciliary dysfunction and can affect an organ system or tissues. Isolated or syndromic retinal dystrophies are the most common ocular manifestation of ciliopathies. The photoreceptor connecting cilium plays a leading role in these ciliopathy-related retinal dystrophies. Dysfunctional photoreceptor cilia cause the most severe type of retinal dystrophy: Leber's congenital amaurosis (LCA). The most common syndromic ciliopathies with an ocular manifestation are Bardet-Biedl syndrome (BBS) and Usher syndrome. Molecular-genetic analysis revealed a large number of cilia genes with a high phenotype heterogeneity. Diagnosis of ciliopathies require a multi-disciplinary approach. Causative treatment of ciliopathies is not yet available; therefore, rehabilitative and supportive treatment is mandatory.
Предметные рубрики MeSH
Abnormalities, MultipleAnimalsAntigens, NeoplasmBardet-Biedl SyndromeCell Cycle ProteinsCerebellumCiliaCiliopathiesCytoskeletal ProteinsDNA Mutational AnalysisDiagnosis, DifferentialDisease Models, AnimalEye AbnormalitiesEye ProteinsGenetic Association StudiesGenetic Diseases, X-LinkedGenotypeHumansKidney Diseases, CysticLeber Congenital AmaurosisMiceMicrotubule-Associated ProteinsMyosin VIIaMyosinsNeoplasm ProteinsOptic Atrophies, HereditaryProteinsRetinaRetinal DystrophiesRetinitis PigmentosaUsher Syndromes