👤 Leman Kayaş

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Emine Çamtosun, Ayşehan Akıncı, Leman Kayaş +2 more · 2023 · Journal of clinical research in pediatric endocrinology · added 2026-04-24
Variants of the melanocortin-4 receptor (
📄 PDF DOI: 10.4274/jcrpe.galenos.2021.2021.0158
MC4R
Nurdan Çiftci, Leman Kayaş, Emine Çamtosun +1 more · 2022 · Journal of clinical research in pediatric endocrinology · added 2026-04-24
The enzyme 17-β-hydroxysteroid dehydrogenase type 3 (17β-HSD3) catalyzes the biosynthesis of testosterone (T) from Δ4-androstenedione, and plays an important role in the final steps of androgen synthe Show more
The enzyme 17-β-hydroxysteroid dehydrogenase type 3 (17β-HSD3) catalyzes the biosynthesis of testosterone (T) from Δ4-androstenedione, and plays an important role in the final steps of androgen synthesis. 17β-HSD3 deficiency originates from mutations in the HSD17B gene, causing an autosomal recessive 46,XY sex developmental disorder (DSD). Patients with 46,XY karyotype can exhibit a wide phenotypic spectrum, varying from complete external female genitalia to male genitalia with hypospadias. Here we report a case of 17β-HSD3 deficiency diagnosed in the infantile period who was later found to have a novel Show less
📄 PDF DOI: 10.4274/jcrpe.galenos.2020.2020.0249
HSD17B12