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  • Czech Society of Ophthalmology of the CzMA  (2)
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  • Czech Society of Ophthalmology of the CzMA  (2)
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  • 1
    Online Resource
    Online Resource
    Czech Society of Ophthalmology of the CzMA ; 2019
    In:  Czech and Slovak Ophthalmology Vol. 75, No. 5 ( 2019-10-21), p. 272-276
    In: Czech and Slovak Ophthalmology, Czech Society of Ophthalmology of the CzMA, Vol. 75, No. 5 ( 2019-10-21), p. 272-276
    Abstract: Introduction: Achromatopsia is an autosomal recessive retinal disorder with an estimated prevalence ranging from 1 in 30.000 to 50.000. The disease is caused by mutations in six different genes. The aim of the study was to perform molecular genetic analysis in 11 unrelated probands with a clinical diagnosis of achromatopsia and to describe clinical findings in those that were found to carry biallelic pathogenic mutations. Methods: All probands and their parents underwent ophthalmic examination. Mutation detection was performed using Sanger sequencing of CNGB3 exons 6, 7, 9-13, which have been found to harbour most diseasecausing mutations in patients with achromatopsia of European origin. Results: Three known pathogenic variants in CNGB3 were identified in 2 probands. Proband 1 was a compound heterozygote for the c.819_826del; p.(Arg274Valfs*13) and c.1006G 〉 T; p.(Glu336*). Proband 2 carried the c.1148del; p.(Thr383Ilefs*13) in a homozygous state. The best corrected visual acuity in proband 1 (aged 19 years) was 0.1 in both eyes, in proband 2 (aged 8 years) 0.05 in the right eye and 0.1 in the left eye. Both individuals had nystagmus, photophobia, and absence of colour discrimination. Fundus examination appeared normal however spectral-domain optical coherence tomography revealed subtle bilaterally symmetrical structural changes in the fovea. Conclusion: Molecular genetic analysis of Czech patients with achromatopsia was performed for the first time. Identification of diseasecausing mutations in achromatopsia is important for establishing an early diagnosis, participation in clinical trials assessing gene therapies and may be also used for preimplantation genetic diagnosis.
    Type of Medium: Online Resource
    ISSN: 1805-4447 , 1211-9059
    URL: Issue
    Language: English
    Publisher: Czech Society of Ophthalmology of the CzMA
    Publication Date: 2019
    Location Call Number Limitation Availability
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  • 2
    Online Resource
    Online Resource
    Czech Society of Ophthalmology of the CzMA ; 2022
    In:  Czech and Slovak Ophthalmology Vol. 78, No. 5 ( 2022-6-27), p. 242-248
    In: Czech and Slovak Ophthalmology, Czech Society of Ophthalmology of the CzMA, Vol. 78, No. 5 ( 2022-6-27), p. 242-248
    Abstract: Aim: Mutations in the myocilin gene (MYOC) cause trabecular dysfunction and thus are involved in the pathogenesis of primary open-angle glaucoma (POAG). The aim of this study was to characterize and describe the clinical findings in two Czech families with POAG due to pathogenic variants in the MYOC gene. Material and methods: Members of the two families affected by POAG underwent complete ophthalmological examination. In the proband from the first family, a direct sequencing of the three most frequent mutations in the MYOC gene was performed, and in the proband from the second family, an exome sequencing was performed. Other family members underwent targeted tests using direct sequencing. Results: In total, 10 individuals diagnosed with POAG aged 20–70 years (mean 32.2 years, SD ±10.9 years) were examined. Eight of them showed advanced glaucomatous neuropathy with severe changes in the retinal nerve fiber layer. Clinical signs of POAG were present in six individuals in the third decade of life already; another four developed POAG during the fourth decade of life. Eight out of 10 patients had to undergo filtration surgery. Surgery was performed within 1 to 7 years of diagnosis, but mostly was performed within 2 years of glaucoma diagnosis. In the first family, MYOC variant c.1099G 〉 A p.(Gly367Arg) was shown in the affected family members; in the second family MYOC variant c.1440C 〉 A p.(Asn480Lys), both in heterozygous state. The changes were assessed as pathogenic. Conclusion: Our study is the first to describe mutations in the MYOC gene causing POAG in Czech patients. Genetic testing may be recommended for this diagnosis, especially in individuals with early presentation and a positive family history. Carriers of pathogenic variants of the MYOC gene have a lifetime risk of developing POAG of more than 50% and the course of their disease is often more aggressive, requiring surgical intervention to permanently control the intraocular pressure.
    Type of Medium: Online Resource
    ISSN: 1805-4447 , 1211-9059
    URL: Issue
    Language: English
    Publisher: Czech Society of Ophthalmology of the CzMA
    Publication Date: 2022
    Location Call Number Limitation Availability
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