Zobrazeno 1 - 10
of 2 229
pro vyhledávání: '"AMBIGUOUS GENITALIA"'
Publikováno v:
Urology Case Reports, Vol 54, Iss , Pp 102707- (2024)
In less than 10% of cases, males may have isolated epispadias, which is caused by failure in the urethral tubularization process, leading to dorsal urethral defect. This case report presents a unique instance where epispadias was associated with ambi
Externí odkaz:
https://doaj.org/article/3174a4a0bf4a4d7d98262cf11f8ba400
Publikováno v:
International Journal of Reproductive BioMedicine, Vol 21, Iss 12, Pp 985-994 (2024)
Abstract Background: A mismatch between chromosomal, gonadal, and phenotypic sexes in individuals with androgen insensitivity syndrome (AIS) creates problems in sex assignment and psychosexual identification. Objective: To identify psychosexual and s
Externí odkaz:
https://doaj.org/article/119efd593b934f3a9274df2603a552f7
Publikováno v:
Radiology Case Reports, Vol 18, Iss 7, Pp 2354-2358 (2023)
Congenital malformations of the urogenital system with fully developed duplications, such as urinary bladder, are sporadic. They are often present in the setting of endogenous molecular disbalance, such as steroid metabolism disturbances. Other rare
Externí odkaz:
https://doaj.org/article/6ebae4f529b94e6eaa9240a0ca745b23
Publikováno v:
Annals of Pediatric Surgery, Vol 19, Iss 1, Pp 1-10 (2023)
Abstract Background Y-type urethral duplication is a term frequently used to describe a rare condition in the male associated with double urinary stream: a weak interrupted urinary stream through a hypoplastic penile urethra, while the main urine flo
Externí odkaz:
https://doaj.org/article/3c4bed810efc4d258ce4ad816ec25963
Publikováno v:
Urology Case Reports, Vol 51, Iss , Pp 102572- (2023)
Differences of sexual development (DSD) refers to congenital conditions characterized by discordant appearances of external genitalia with respect to sex chromosomes. We present a case of a 46 XY DSD adolescent with bilateral undescended testes and s
Externí odkaz:
https://doaj.org/article/444207f2b4a34edabfe286c03d000b5b
Publikováno v:
International Medical Case Reports Journal, Vol Volume 16, Pp 193-199 (2023)
Telila Mesfin,1 Nuri Haji,1 Fikadu Seyoume,2 Kenbon Seyoum,3 Eshetu Mesfin,4 Tsegaye Erdachew,5 Daniel Ayane,5 Gadisa Badasa,5 Moisan Soboka5 1Department of Medicine, Madda Walabu University Goba General Hospital, Goba, Ethiopia; 2Department of Pedia
Externí odkaz:
https://doaj.org/article/574592b3432f4044b2ce2dfa9920f122
Autor:
Özge Köprülü, Sezer Acar, Kadri Murat Erdoğan, Özlem Nalbantoğlu, Tarık Kırkgöz, Gülçin Arslan, Beyhan Özkaya, Yaşar Bekir Kutbay, Behzat Özkan
Publikováno v:
Journal of Pediatric Research, Vol 9, Iss 4, Pp 401-408 (2022)
The 45,X/47,XYY mosaicism is an extremely rare genetic disorder with highly phenotypic manifestations such as ovotesticular disorders of sexual development, mixed gonadal dysgenesis and Turner syndrome. Herein, we report two cases with very distincti
Externí odkaz:
https://doaj.org/article/ac925d37e44443fb9c358adf8d8c2b2a
Autor:
Amanda Trixie Hardigaloeh, Tri Juli Edi Tarigan, Em Yunir, Kanadi Sumapradja, Feranindhya Agiananda, Yulia Ariani, Nanis S Marzuki, Irfan Wahyudi, Lisnawati Lisnawati
Publikováno v:
Acta Medica Indonesiana, Vol 55, Iss 4 (2023)
A 19-year-old girl was referred with delayed puberty and ambiguous genitalia. She had short stature with high blood pressure and Turner’s stigmata with external genitalia Prader Score 4. Ultrasound revealed hypoplastic uterus with no gonad. Follicl
Externí odkaz:
https://doaj.org/article/a3d6fb3ad3e9431bbc4e27d14cc31915
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