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S. Kaygusuz

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Case report Open access Oct 2026

Rare SERPINH1 and SERPINF1 Variants in Autosomal Recessive Osteogenesis Imperfecta Type X and Type VI.

Osteogenesis imperfecta (OI) is a group of connective tissue disorders characterized by bone fragility and low bone mineral density (BMD). Two severe autosomal recessive forms, OI type X and VI, can be caused by variants in the SERPINH1 and SERPINF1 genes, respectively. In this study, we reported two children from two...

Fan Wang, A. Costantini, S. Kaygusuz et al. · 0 citations
Sep 2026

Anti-Müllerian hormone levels in girls with precocious puberty

Abstract Objectives We aimed to evaluate the relationship between anti-Müllerian hormone (AMH) levels in cases of central precocious puberty (CPP), premature adrenarche (PA), and isolated premature thelarche (IPT) and those of healthy controls (HC). Methods A total of 153 girls (40 PA, 39 CPP, 39 IPT, and 35 HC) were i...

M. Hepokur, A. Çamaş, Gozde Tanis et al. · 0 citations

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