Zobrazeno 1 - 10
of 217
pro vyhledávání: '"Genital Ambiguity"'
Publikováno v:
مجله دانشگاه علوم پزشکی گرگان, Vol 25, Iss 1, Pp 104-119 (2023)
Hermaphrodite patients are individuals who, due to various issues such as chromosomal, gonadal or hormonal disorders that occurred during pregnancy, experience physiological abnormalities in their genital area after birth. As a result, they may have
Externí odkaz:
https://doaj.org/article/23e9583f9880431ab639f573caecedbd
Akademický článek
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Autor:
Chiara Simeoli, Cristina de Angelis, Alessandra Delli Veneri, Davide Menafra, Nicola Di Paola, Claudia Pivonello, Carolina Di Somma, Paolo Valerio, Daniela Melis, Carlo Alviggi, Annamaria Colao, Rosario Pivonello
Publikováno v:
Frontiers in Genetics, Vol 13 (2022)
Congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency (21-OHD) represents the most frequent form of CAH and of 46, XX disorder of sex development in female newborns. In the majority of cases, particularly in developed countries, femal
Externí odkaz:
https://doaj.org/article/3ce418788b884590885890a8a95b7479
Publikováno v:
Journal of Indian Association of Pediatric Surgeons, Vol 24, Iss 3, Pp 162-169 (2019)
Disorders of sex development (DSD) are a sensitive and stressful condition for the family as well as the treating physician to deal with. The main issue in managing such cases is sex assignment. The decision is influenced by the cultural background,
Externí odkaz:
https://doaj.org/article/c4356048ae4d4d39892393716487c3fe
Autor:
Simeoli, Chiara, de Angelis, Cristina, Delli Veneri, Alessandra, Menafra, Davide, Di Paola, Nicola, Pivonello, Claudia, Di Somma, Carolina, Valerio, Paolo, Melis, Daniela, Alviggi, Carlo, Colao, Annamaria, Pivonello, Rosario
Publikováno v:
Frontiers in Genetics. 13
Congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency (21-OHD) represents the most frequent form of CAH and of 46, XX disorder of sex development in female newborns. In the majority of cases, particularly in developed countries, femal
Autor:
Maria-Grazia Scarpa
Publikováno v:
Frontiers in Pediatrics, Vol 5 (2017)
Externí odkaz:
https://doaj.org/article/396fdbcff162464fb729d3e0143d0fce
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 2, Iss 4, Pp 292-296 (2014)
Abstract Inactivating mutations of the 5α‐steroid reductase type‐2 (SRD5A2) gene result in a broad spectrum of masculinization defects, ranging from a male phenotype with hypospadias to a female phenotype with Wolffian structures. Molecular stud
Externí odkaz:
https://doaj.org/article/f70d5067d37843be938c4a884e0de9a2
Autor:
Sajni I Khemchandani
Publikováno v:
Journal of Indian Association of Pediatric Surgeons, Vol 20, Iss 2, Pp 84-86 (2015)
The diagnosis and management of a child with ambiguous genitalia and severe variety of urogenital sinus with a high vesico-vaginal confluence is challenging. This 4-year-old female child had solitary right kidney with ectopic ureter opening in high v
Externí odkaz:
https://doaj.org/article/582ddee82fe74d54b32db2d3dfe1c9bf
Autor:
Jatinder Kumar, Vikas Kumar, Vijaylakshmi Bhatia, Preeti Dabadghao, Samit Chaturvedi, Rakesh Kapoor, M S Ansari
Publikováno v:
Indian Journal of Urology, Vol 28, Iss 3, Pp 286-291 (2012)
Introduction: Ambiguous genitalia are a major cause of parental anxiety and create psychological and social problems to patient, if not managed properly. Here we present our experience in managing patients with ambiguous genitalia. Material and Metho
Externí odkaz:
https://doaj.org/article/2f4f2f58a47b4923b99ac8d32fff5def
Publikováno v:
Arquivos Brasileiros de Psicologia, Vol 63, Iss 2, Pp 82-91 (2011)
This research aimed to know and understand the actions involved in health care for patients with genital ambiguity in a General Hospital located in the Brazilian Northeast. The methodology consisted of surveying data from medical records to identify
Externí odkaz:
https://doaj.org/article/2521f3a976c542beab0db9072a885902