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Long‐term outcome of ovotesticular disorder of sex development: A single center experience
International Journal of Urology, 2011Objectives: To describe the clinical features of children with ovotesticular disorder of sex development (DSD) and to review cases of ovotesticular DSD in Japan.Methods: Medical records of eight children diagnosed with ovotesticular DSD at our institute during the past 17 years were retrospectively evaluated.
Futoshi, Matsui +6 more
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The Genetics of Ovotesticular Disorders of Sex Development
2011Disorders of sex development (DSD) encompass a very large spectrum of phenotypes, from minor malformations of the genitalia (hypospadias, cryptorchidism, and hypertrophy of the clitoris) to sexual ambiguity. Taken altogether, these anomalies have an estimated frequency of 0.5–1%.
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Regional Variations in the Management of Testicular or Ovotesticular Disorders of Sex Development
Sexual Development, 2011Disorders of sex development arise in parts of the world with different socio-economic and cultural characteristics. We wished to determine the regional variations in the management of these conditions. A questionnaire was e-mailed to the 650 members of the European Society for Paediatric Endocrinology (ESPE), an international society with a mainly ...
N, Josso, L, Audi, G, Shaw
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Hormone Research in Paediatrics, 2017
<b><i>Objective:</i></b> To describe the clinical characteristics, biochemistry, histopathology, and long-term outcomes in subjects with ovotesticular (OT) disorder of sex development (DSD). <b><i>Study Design:</i></b> This is a retrospective subset analysis of 64 cases of histologically confirmed OT DSD.
Yasmeen, Ganie +3 more
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<b><i>Objective:</i></b> To describe the clinical characteristics, biochemistry, histopathology, and long-term outcomes in subjects with ovotesticular (OT) disorder of sex development (DSD). <b><i>Study Design:</i></b> This is a retrospective subset analysis of 64 cases of histologically confirmed OT DSD.
Yasmeen, Ganie +3 more
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Long-Term Followup of a Large Cohort of Patients with Ovotesticular Disorder of Sex Development
Journal of Urology, 2014We present the followup of a large cohort of patients with ovotesticular disorder of sex development treated at a single tertiary center.We reviewed the records of 20 patients with ovotesticular disorder of sex development. We retrospectively evaluated clinical and surgical characteristics.
Maria Helena Palma, Sircili +8 more
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Pediatric and Developmental Pathology, 2018
Simpson–Golabi–Behmel syndrome type I (SGBS, OMIM312870), caused by defects of the GPC3 and GPC4 genes on chromosome Xq26, is an X-linked recessive macrosomia/multiple congenital anomaly disorder characterized by somatic overgrowth, coarse facial features, variable congenital anomalies, increased tumor risk, and mild-to-moderate neurodevelopmental ...
Monique E, De Paepe +3 more
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Simpson–Golabi–Behmel syndrome type I (SGBS, OMIM312870), caused by defects of the GPC3 and GPC4 genes on chromosome Xq26, is an X-linked recessive macrosomia/multiple congenital anomaly disorder characterized by somatic overgrowth, coarse facial features, variable congenital anomalies, increased tumor risk, and mild-to-moderate neurodevelopmental ...
Monique E, De Paepe +3 more
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Urology, 2019
A 53-year-old male referred to our centre because of hypergonadotropic hypogonadism detected during urological follow-up for urethral lithiasis. Physical examination showed short stature, micropenis, ambiguous external genitalia, and normal secondary sexual characteristics. Karyotype: 45 × 0/46XY.
Caputo M. +8 more
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A 53-year-old male referred to our centre because of hypergonadotropic hypogonadism detected during urological follow-up for urethral lithiasis. Physical examination showed short stature, micropenis, ambiguous external genitalia, and normal secondary sexual characteristics. Karyotype: 45 × 0/46XY.
Caputo M. +8 more
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[Diagnosis and treatment of ovotesticular disorders of sex development in children].
Zhonghua nan ke xue = National journal of andrology, 2009To investigate the diagnosis and treatment of ovotesticular disorders of sex development (DSD) in children.We reviewed the clinical data of 9 cases of ovotesticular DSD admitted in our department from 1988 to 2007.The patients ranged in age from 9 months to 9 years, 7 raised as males and 2 as females. As for the karyotype, 4 cases were 46,XX, 2 were 46,
Liang-Sheng, Lu +6 more
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Ovotesticular disorder of sex development: A rare cause of gynecomastia
Clinical History: A 13-year-old patient, raised as a boy, presented with gynecomastia and left-sided groin pain. On examination, the left scrotal sac was empty, with tenderness in the left groin. Pubic and axillary hair were present, and external genitalia consisted of a penis with hypospadias (Figures 1b and c).openaire +1 more source

