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  1. Article ; Online: Clinical and genetic characteristics and natural history of Finnish families with familial exudative vitreoretinopathy due to pathogenic FZD4 variants.

    Lähteenoja, Laura / Palosaari, Tapani / Tiirikka, Timo / Haanpää, Maria / Moilanen, Jukka / Falck, Aura / Rahikkala, Elisa

    Acta ophthalmologica

    2024  

    Abstract: Purpose: To report clinical and genetic characteristics of familial exudative vitreoretinopathy (FEVR) in the Finnish population.: Methods: Detailed clinical and genetic data of 35 individuals with heterozygous pathogenic variants in FZD4 were ... ...

    Abstract Purpose: To report clinical and genetic characteristics of familial exudative vitreoretinopathy (FEVR) in the Finnish population.
    Methods: Detailed clinical and genetic data of 35 individuals with heterozygous pathogenic variants in FZD4 were gathered and analysed.
    Results: Thirty-two individuals with FZD4 c.313A>G variant and three individuals with FZD4 c.40_49del were included in the study. The clinical phenotype was variable even among family members with the same FZD4 variant. Only 34% (N = 12/35) of variant-positive individuals had been clinically diagnosed with FEVR. The median age of the onset of symptoms was 2.3 years, ranging between 0 to 25 years. Median visual acuity was 0.1 logMAR (0.8 Snellen decimal), ranging between light perception and -0.1 logMAR (1.25 Snellen decimal). Most (N = 33/35, 94%) were classified as not visually impaired. Despite unilateral visual loss present in some, they did not meet the criteria of visual impairment according to the WHO classification. Two study patients (N = 2/35, 6%) had severe visual impairment. The most common FEVR stage in study patient's eyes (N = 28/70 eyes, 40%) was FEVR stage 1, that is, avascular periphery or abnormal vascularisation. Most of FZD4-variant-positive study patient's eyes (N = 31/50 eyes, 62%) were myopic. Two individuals presented with persistent hyperplastic primary vitreous expanding the phenotypic spectrum of FEVR. Shared haplotypes extending approximately 0.9 Mb around the recurrent FZD4 c.313A>G variant were identified.
    Conclusion: Most study patients were unaffected or had mild clinical manifestations by FEVR. Myopia seemed to be overly common in FZD4-variant-positive individuals.
    Language English
    Publishing date 2024-05-05
    Publishing country England
    Document type Journal Article
    ZDB-ID 2408333-1
    ISSN 1755-3768 ; 1755-375X
    ISSN (online) 1755-3768
    ISSN 1755-375X
    DOI 10.1111/aos.16701
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: A novel frameshift variant in

    Lähteenoja, Laura / Häkli, Sanna / Tuupanen, Sari / Kuismin, Outi / Palosaari, Tapani / Rahikkala, Elisa / Falck, Aura

    Ophthalmic genetics

    2022  Volume 43, Issue 2, Page(s) 152–158

    Abstract: Background: Pathogenic variants in the : Materials and methods: Our patients were first discovered in a registry-based study. Later, they gave their written consent for this study. In order to describe the genotype and phenotype, their historic ... ...

    Abstract Background: Pathogenic variants in the
    Materials and methods: Our patients were first discovered in a registry-based study. Later, they gave their written consent for this study. In order to describe the genotype and phenotype, their historic clinical patient data and genetic data were gathered, and a clinical ophthalmic examination and an audiogram were performed. For this review, a PubMed search using the keyword CEP78 was carried out. The first article on
    Results: A large gene panel identified a homozygous
    Conclusions: Here, we present a comprehensive review of
    MeSH term(s) Cell Cycle Proteins/genetics ; Frameshift Mutation ; Humans ; Mutation ; Pedigree ; Phenotype ; Retinitis Pigmentosa/genetics ; Retinitis Pigmentosa/pathology ; Usher Syndromes/genetics
    Chemical Substances CEP78 protein, human ; Cell Cycle Proteins
    Language English
    Publishing date 2022-03-03
    Publishing country England
    Document type Journal Article ; Review ; Research Support, Non-U.S. Gov't
    ZDB-ID 1199279-7
    ISSN 1744-5094 ; 0167-6784 ; 1381-6810
    ISSN (online) 1744-5094
    ISSN 0167-6784 ; 1381-6810
    DOI 10.1080/13816810.2022.2045511
    Database MEDical Literature Analysis and Retrieval System OnLINE

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