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Laparoscopic evaluation and treatment of the impalpable testis
(2001-01-01)
Objectives: To evaluate the laparoscopic technique as a diagnostic and therapeutic tool in the management of patients with impalpable testis. Material and Methods: Fifty-nine patients with mean age of 6.3 years underwent ...
Laparoscopic evaluation and treatment of the impalpable testis
(2001-01-01)
Objectives: To evaluate the laparoscopic technique as a diagnostic and therapeutic tool in the management of patients with impalpable testis. Material and Methods: Fifty-nine patients with mean age of 6.3 years underwent ...
Crossed testicular ectopia
(Associação Paulista de Medicina - APM, 1995-08-01)
Crossed testicular ectopia (CTE) is a rare anomaly, characterized by migration of one testis towards the opposite inguinal canal. Presented here is a case of crossed ectopia of the right testis, treated by extraperitoneal ...
Early orchiopexy to prevent germ cell loss during infancy in congenital cryptorchidism
(Endocrine Society, 2012-12)
Cryptorchidism is a problematic topic, beginning with its meaning. Although, by etymology, it refers to “hidden testes,” the term cryptorchidism has been widely used to describe testes that are not in their normal position ...
Crossed testicular ectopia
(John Wiley and Sons Ltd, 2010)
Crossed testicular ectopia is a low-prevalence entity. It consists of a congenital abnormality in which both testicles are located in the same inguinal cord or scrotal sac with independent irrigation. It may be suspected ...
Intra-abdominal Sertoli Cell Tumor in Dog with Local and Systemic Repercussions
(Universidade Federal do Rio Grande do Sul, 2018)
Sertolioma in a Canadian Husky: Relationship between Tumor, Hormones, Neurons and Skin
(Universidade Federal do Rio Grande do Sul, 2019)
A Novel Anti-Mullerian Hormone (AMH) Gene Mutation in a Patient with Persistent Müllerian Duct Syndrome (PMDS) type 1
(Karger, 2019)
PMDS is an autosomic recessive disorder of sexual development caused by inactivating mutations in the AMH or the AMH receptor gene (PMDS type I and II respectively). This condition leads to the persistence of Müllerian ...