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[Ciliopathies].
- Source :
-
Klinische Monatsblatter fur Augenheilkunde [Klin Monbl Augenheilkd] 2018 Mar; Vol. 235 (3), pp. 264-272. Date of Electronic Publication: 2018 Mar 13. - Publication Year :
- 2018
-
Abstract
- 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.<br />Competing Interests: Die Autoren geben an, dass kein Interessenkonflikt besteht.<br /> (Georg Thieme Verlag KG Stuttgart · New York.)
- Subjects :
- Abnormalities, Multiple diagnosis
Abnormalities, Multiple genetics
Abnormalities, Multiple physiopathology
Animals
Antigens, Neoplasm genetics
Bardet-Biedl Syndrome diagnosis
Bardet-Biedl Syndrome genetics
Bardet-Biedl Syndrome physiopathology
Cell Cycle Proteins
Cerebellum abnormalities
Cerebellum physiopathology
Cilia physiology
Ciliopathies genetics
Ciliopathies physiopathology
Cytoskeletal Proteins
DNA Mutational Analysis
Diagnosis, Differential
Disease Models, Animal
Eye Abnormalities diagnosis
Eye Abnormalities genetics
Eye Abnormalities physiopathology
Eye Proteins genetics
Genetic Association Studies
Genetic Diseases, X-Linked diagnosis
Genetic Diseases, X-Linked genetics
Genetic Diseases, X-Linked physiopathology
Genotype
Humans
Kidney Diseases, Cystic diagnosis
Kidney Diseases, Cystic genetics
Kidney Diseases, Cystic physiopathology
Leber Congenital Amaurosis diagnosis
Leber Congenital Amaurosis genetics
Leber Congenital Amaurosis physiopathology
Mice
Microtubule-Associated Proteins genetics
Myosin VIIa
Myosins genetics
Neoplasm Proteins genetics
Optic Atrophies, Hereditary diagnosis
Optic Atrophies, Hereditary genetics
Optic Atrophies, Hereditary physiopathology
Proteins genetics
Retina abnormalities
Retina physiopathology
Retinal Dystrophies genetics
Retinal Dystrophies physiopathology
Retinitis Pigmentosa diagnosis
Retinitis Pigmentosa genetics
Retinitis Pigmentosa physiopathology
Usher Syndromes diagnosis
Usher Syndromes genetics
Usher Syndromes physiopathology
Ciliopathies diagnosis
Retinal Dystrophies diagnosis
Subjects
Details
- Language :
- German
- ISSN :
- 1439-3999
- Volume :
- 235
- Issue :
- 3
- Database :
- MEDLINE
- Journal :
- Klinische Monatsblatter fur Augenheilkunde
- Publication Type :
- Academic Journal
- Accession number :
- 29534263
- Full Text :
- https://doi.org/10.1055/a-0573-9199