Search Results - "disorders of sex development"

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  1. 81
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    Clinical, endocrinological, and molecular features of four Korean cases of cytochrome P450 oxidoreductase deficiency by Yena Lee, Jin-Ho Choi, Arum Oh, Gu-Hwan Kim, Sook-Hyun Park, Jung Eun Moon, Cheol Woo Ko, Chong-Kun Cheon, Han-Wook Yoo

    Published 2020
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  2. 82
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    Prevalence and risk factors of testicular microlithiasis in patients with hypospadias: a retrospective study by Michiko Nakamura, Kimihiko Moriya, Yoko Nishimura, Mutsumi Nishida, Yusuke Kudo, Yukiko Kanno, Takeya Kitta, Masafumi Kon, Nobuo Shinohara

    Published 2018
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  3. 83
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    46,XY Sex Development Defect due to a Novel Homozygous (Splice Site) c.673_1G>C Variation in the HSD17B3 Gene: Case Report by Nurdan Çiftci, Leman Kayaş, Emine Çamtosun, Ayşehan Akıncı

    Published 2022
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  4. 84
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    Primary Adrenal Insufficiency, Complete Sex Reversal, and Unique Clinical Phenotype in a Patient with Severe CYP11A1 (P450scc) Deficiency-Case Report and Literature Overview by Zuzanna Nowak, Ewelina Preizner-Rzucidło, Jakub Gawlik, Jerzy B. Starzyk, Dominika Januś

    Published 2024
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  5. 85
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    Clinical and hormonal characteristics and growth data of 45,X/46,XY mosaicism in 38 Chinese patients by Jiaoru Yang, Yan Li, Pin Li

    Published 2023
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  6. 86
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    Clinical, hormonal and genetic characteristics of androgen insensitivity syndrome in 39 Chinese patients by Qingxu Liu, Xiaoqin Yin, Pin Li

    Published 2020
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  7. 87
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    Growth Pattern in Chinese Children With 5α-Reductase Type 2 Deficiency: A Retrospective Multicenter Study by Xiu Zhao, Xiu Zhao, Yanning Song, Shaoke Chen, Xiumin Wang, Feihong Luo, Yu Yang, Linqi Chen, Ruimin Chen, Hui Chen, Zhe Su, Di Wu, Chunxiu Gong

    Published 2019
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  8. 88
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    Mutations in AR or SRD5A2 Genes: Clinical Findings, Endocrine Pitfalls, and Genetic Features of Children with 46,XY DSD by Neşe Akcan, Oya Uyguner, Firdevs Baş, Umut Altunoğlu, Güven Toksoy, Birsen Karaman, Şahin Avcı, Zehra Yavaş Abalı, Şükran Poyrazoğlu, Agharza Aghayev, Volkan Karaman, Rüveyde Bundak, Seher Başaran, Feyza Darendeliler

    Published 2022
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  9. 89
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    Prevalência de anormalidades genitais em recém-nascidos Prevalence of genital abnormalities in neonates by Isabella L. Monlleó, Susane V. Zanotti, Bárbara Priscila B. de Araújo, Erisvaldo F. Cavalcante Júnior, Paula D. Pereira, Paulo M. de Barros, Maria Deysiane P. Araújo, Ana Thaysa V. S. de Mendonça, Catarina R. S. Santos, Ylana R. dos Santos, Débora de Paula Michelatto, Maricilda P. de Mello, Andrea T. Maciel-Guerra, Gil Guerra-Júnior

    Published 2012
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  10. 90
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    MYRF mutation leads to a single manifestation of sexual development and mimics partial androgen insensitivity syndrome: a case report and literature review by Duoduo Zhang, Qinjie Tian

    Published 2024
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  11. 91
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    Pituitary Macroadenoma in a Girl with Male Karyotype: A Rare Case Study by Fatinah Shahab, Tania Tedjo Minuljo, Calvin Layuk Allo, Dody Priambada, Mahayu Dewi Ariani, Sultana Faradz

    Published 2023
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  12. 92
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    Phenotypic variability and management of patients with mosaic monosomy X and Y chromosome material: a case series by Myriam Ben Fredj, Marwa Messaoud, Sabrine Ben Youssef, Salma Mani, Syrine Laaribi, Rania Sakka, Hayet Ben Hmida, Amine Ksiaa, Mongi Mekki, Mohsen Belghith, Lassaad Sahnoun

    Published 2024
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  13. 93
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    Barriers in access to healthcare services for individuals with disorders of sex differentiation in Bangladesh: an analysis of regional representative cross-sectional data by Alam Khan, T. M. Fahad, Md Imran Nur Manik, Hazrat Ali, Md. Ashiquazzaman, Md Ibrahim Mollah, Tanjeena Zaman, Md Shariful Islam, Moizur Rahman, Aminur Rahman, Mostafizur Rahman, Tarannum Naz, Mahmud Arif Pavel, Md. Nuruzzaman Khan

    Published 2020
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  14. 94
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    46 xy ovotesticular disorder: A rare case report with review of literature by Bhati Meenal, Gothwal Meenakshi, Singh Pratibha, Yadav Garima, Kathuria Priyanka, Elhence Poonam

    Published 2021
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  15. 95
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    Complete Androgen Insensitivity Syndrome: A Rare Case of Prenatal Diagnosis by Maria Liz Coelho, Elisa Soares, Marília Freixo, Pedro Brandão, Carla Marinho, Juliana Rocha, Graça Rodrigues

    Published 2021
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  16. 96
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    A rare case of swyer syndrome in two sisters with successful pregnancy outcome in both by Anupam Gupta, Ritika Bajaj, Umesh N Jindal

    Published 2019
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  17. 97
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    Complete androgen insensitivity syndrome: A rare case report by Tushar Kambale, Payal Patel, Yaminy Pradeep Ingale, Charusheela Gore

    Published 2022
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  18. 98
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    The role of sex hormones in physiological adaptation and athletic performance in women with hyperandrogenism: medical and ethical aspects by Aleksandra Kępczyńska, Kamil Górecki, Przemysław Prokop, Konrad Barszczewski, Urszula Korzonek

    Published 2024
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  19. 99
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    Bilateral sactosalphinx and congenital adrenal hyperplasia: case report on two rare conditions in two virgin girls by Maria-Grazia Scarpa, Marianna Iaquinto, Daniela Codrich, Jürgen Schleef

    Published 2021
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  20. 100
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    Enduring uncertainties. Medical accounts on caring for young people with variations of sex characteristics by Nina Reber, Eva De Clercq

    Published 2022
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