National Repository of Grey Literature 3 records found  Search took 0.00 seconds. 
Developmental disorders of the lens and anterior segment of the eye
Jedličková, Jana ; Ďuďáková, Ľubica (advisor) ; Šafka Brožková, Dana (referee) ; Cvekl, Ales (referee)
The anterior segment of the eye includes the eyelids, eyelashes, tear film, cornea, conjunctiva, iris, pupil, ciliary body, chamber angle, and lens. Cataracts and anterior segment dysgenesis are a highly heterogeneous group of diseases exhibiting all types of Mendelian inheritance. The aim of this thesis was molecular genetic analysis of 51 patients from 23 families with congenital and early onset cataracts and/or anterior segment dysgenesis, using a modern as well as conventional methods, such as next-generation sequencing, direct sequencing, bioinformatic and functional analyses including the use of artificial splicing vectors. We identified 24 causal variants in the coding, non-coding and regulatory regions of the PAX6, FTL, FOXC1, PITX2, FOXE3, and CHRDL1 genes. We confirmed the role of the n.37C>T variant in MIR204 in the development of chorioretinal dystrophy variably associated with iris coloboma, early-onset cataracts and congenital glaucoma. Splicing assay confirmed pathogenic effect of two mutations on pre-mRNA splicing of the PAX6 gene. Establishing molecular genetics diagnosis improves patient counselling and their relatives in terms of the prognosis and risk of developing secondary glaucoma Key words: molecular-genetic diagnosis, anterior segment dysgenesis, next-generation sequencing,...
Linkage analyses and characterization of candidate gene locuses and genes in families with multiple appearance of hereditary neuropathy Charcot-Marie-Tooth or deafness with unexplained gene defect
Šafka Brožková, Dana ; Seeman, Pavel (advisor) ; Kemlink, David (referee) ; Fajkusová, Lenka (referee)
Topics of the Ph.D. studies were: 1) hereditary neuropathy and 2) non-syndromic hearing loss Ad 1) The larger part of the dissertation thesis is devoted to hereditary neuropathies Charcot-Marie-Tooth (CMT). Four families with hereditary neuropathy were examined by the linkage analysis on SNP chips. The other part describe the analysis of new mutations in the GJB1, MPZ and PMP22 genes. Ad 2) The author performed the homozygosity mapping in a Czech Roma families with non-syndromic hearing loss.
Linkage analyses and characterization of candidate gene locuses and genes in families with multiple appearance of hereditary neuropathy Charcot-Marie-Tooth or deafness with unexplained gene defect
Šafka Brožková, Dana ; Seeman, Pavel (advisor) ; Kemlink, David (referee) ; Fajkusová, Lenka (referee)
Topics of the Ph.D. studies were: 1) hereditary neuropathy and 2) non-syndromic hearing loss Ad 1) The larger part of the dissertation thesis is devoted to hereditary neuropathies Charcot-Marie-Tooth (CMT). Four families with hereditary neuropathy were examined by the linkage analysis on SNP chips. The other part describe the analysis of new mutations in the GJB1, MPZ and PMP22 genes. Ad 2) The author performed the homozygosity mapping in a Czech Roma families with non-syndromic hearing loss.

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