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- W4200301118 abstract "Short telomere syndromes constitute a heterogeneous group of clinical conditions characterized by short telomeres and impaired telomerase activity due to pathogenic variants in the essential telomerase components. Dyskeratosis congenita (DC) is a rare, multisystemic telomere biology disorder characterized by abnormal skin pigmentation, oral leukoplakia and nail dysplasia along with various somatic findings. Hoyeraal-Hreidarsson syndrome (HHS) is generally an autosomal recessively inherited subgroup showing growth retardation, microcephaly, cerebellar hypoplasia and severe immunodeficiency. We here report on a consanguineous family from Turkey, in which a missense variant in the reverse transcriptase domain of the TERT gene segregated with short telomere lengths and was associated with full-blown short telomere syndrome phenotype in the index; and heterogeneous adult-onset manifestations in heterozygous individuals." @default.
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- W4200301118 date "2021-12-09" @default.
- W4200301118 modified "2023-10-16" @default.
- W4200301118 title "Biallelic <i>TERT</i> variant leads to Hoyeraal–Hreidarsson syndrome with additional dyskeratosis congenita findings" @default.
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- W4200301118 doi "https://doi.org/10.1002/ajmg.a.62602" @default.
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