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• W2018451246 abstract "<b><i>Background:</i></b> Heterozygous <i>SOX2</i> mutations have been reported to cause isolated hypogonadotropic hypogonadism (HH) in addition to ocular and brain abnormalities. <b><i>Objective:</i></b> We report a novel missense <i>SOX2</i> (Y110C) mutation in an HH patient with mild ocular malformation. <b><i>Patients:</i></b> The 20-year-old male was referred because of typical signs of complete hypogonadism, with small intrascrotal testes (2 ml), no pubic hair (P1), and a micropenis. Hormone assays revealed very low plasma testosterone levels and very low levels of plasma gonadotropin. He was found to have retinal detachment in his right eye and surgery was performed at the age of 14 years. <b><i>Results:</i></b> Using a next-generation sequencing strategy, we identified a novel heterozygous <i>SOX2</i> mutation, c.329A>G (p.Y110C). Y110C SOX2 had reduced transactivation and no dominant negative effect. Subcellular localization revealed no significant difference between wild-type and mutant SOX2. EMSA experiments showed that the Y110C SOX2 abrogated DNA-binding ability. <b><i>Conclusion:</i></b> The Y110C mutation affects a critical residue in the SOX2 protein. This study extends our understanding of the phenotypic features, molecular mechanism, and developmental course associated with mutations in <i>SOX2</i>. When multiple genes need to be analyzed for mutations simultaneously, targeted sequence analysis of interesting genomic regions is an attractive approach." @default.
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• W2018451246 date "2014-01-01" @default.
• W2018451246 modified "2023-09-24" @default.
• W2018451246 title "A Novel Mutation in SOX2 Causes Hypogonadotropic Hypogonadism with Mild Ocular Malformation" @default.
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• W2018451246 doi "https://doi.org/10.1159/000355279" @default.
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