Zobrazeno 1 - 10
of 2 785
pro vyhledávání: '"virilization"'
Autor:
Somboon Wankanit, Housna Zidoune, Joëlle Bignon-Topalovic, Laurène Schlick, Denis Houzelstein, Leila Fusée, Asma Boukri, Nassim Nouri, Ken McElreavey, Anu Bashamboo, Maëva Elzaiat
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-12 (2024)
Abstract NR2F2 encodes COUP-TFII, an orphan nuclear receptor required for the development of the steroidogenic lineages of the murine fetal testes and ovaries. Pathogenic variants in human NR2F2 are associated with testis formation in 46,XX individua
Externí odkaz:
https://doaj.org/article/77766382aaa847189fa76e3bb2fc1a8f
Autor:
Bas P. H. Adriaansen, Agustini Utari, Dineke Westra, Achmad Zulfa Juniarto, Mahayu Dewi Ariani, Annastasia Ediati, Mariska A. M. Schröder, Paul N. Span, Fred C. G. J. Sweep, Stenvert L. S. Drop, Sultana M. H. Faradz, Antonius E. van Herwaarden, Hedi L. Claahsen – van der Grinten
Publikováno v:
Frontiers in Endocrinology, Vol 15 (2024)
IntroductionCongenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency (21OHD) or 11-hydroxylase deficiency (11OHD) is characterized by underproduction of cortisol and overproduction of adrenal androgens. These androgens lead to a variable
Externí odkaz:
https://doaj.org/article/48f6cb3fd87c455992e4f56a2d178f4c
Autor:
Pastor Escárcega-Fujigaki, Guillermo Hernández-Peredo Rezk, José de Jesús Loeza- Oliva, Anallely Luna-Hernández, Bethsaida Natali Arreguín-Cortés, Rafael López-Cruz
Publikováno v:
Journal of Pediatric Surgery Case Reports, Vol 107, Iss , Pp 102841- (2024)
Introduction: Adrenocortical carcinoma (ACC) is rare, aggressive, and metastasizes mainly to the lungs, liver, and regional lymph nodes. This is the first reported case of a pediatric patient with adrenohepatic fusion (AHF) and functional ACC that so
Externí odkaz:
https://doaj.org/article/70e5907aff35485da55bceed4b26b6dd
Publikováno v:
Frontiers in Oncology, Vol 14 (2024)
ObjectiveTo provide a reference for the diagnosis and treatment of ovarian steroid cell tumors, not otherwise specified (SCTs-NOS).MethodsWe retrospectively analyzed the clinicopathological data of three patients with SCTs-NOS admitted to the Tianjin
Externí odkaz:
https://doaj.org/article/9a138644488d49ef9f929a6bc7800c8d
Autor:
Elena V. Sibirskaya, Irina V. Karachentsova, Angelina A. Sysoeva, Mariia Yu. Chernysheva, Kristina A. Osmanova, Evgenia G. Kotikova
Publikováno v:
Педиатрическая фармакология, Vol 21, Iss 1, Pp 41-49 (2024)
Hormone-producing ovarian tumors in girls are an actual problem in modern gynecology, which is associated with certain difficulties in managing patients. Firstly, it is worth taking into account the higher anatomical mobility of tumors in girls than
Externí odkaz:
https://doaj.org/article/a43dbfa066cc46fea99e567a65846831
Autor:
A Bergougnoux, L Gaspari, M Soleirol, N Servant, S Soskin, S Rossignol, K Wagner-Mahler, J Bertherat, C Sultan, N Kalfa, F Paris
Publikováno v:
Endocrine Connections, Vol 12, Iss 12, Pp 1-9 (2023)
Although hyperandrogenism is a frequent cause of consultation in adolescent girls, more severe forms with virilization must lead to suspicion of an adrenal or ovarian tumor. However, they may also reveal a 46,XY disorder of sexual development (DSD).
Externí odkaz:
https://doaj.org/article/3764aeb463be42a6bebc540b3e30a279
Publikováno v:
AACE Clinical Case Reports, Vol 9, Iss 6, Pp 182-185 (2023)
Background/Objective: Leydig cell tumors are a rare androgen-secreting ovarian tumor. We present a patient with virilization symptoms secondary to a Leydig cell tumor, with nonrevealing imaging studies, that was localized using ovarian vein sampling
Externí odkaz:
https://doaj.org/article/01ca2a2d06994b20870d5157252fc0aa
Publikováno v:
Акушерство, гинекология и репродукция, Vol 17, Iss 4, Pp 462-475 (2023)
The literature review is dedicated to the topical subject in current endocrinology and gynecology – clitoromegaly. At present, clitoromegaly is considered as a symptom of an endocrinological disease associated with impaired testosterone or androgen
Externí odkaz:
https://doaj.org/article/c9d3b15ee59145ddbc55101bd1d90377
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Autor:
Thabitha J. Hoole, Shamaali Gunawardana, Sureshi Nandani Tennekoon, Malik Samarasinghe, Sumudu Nimali Seneviratne
Publikováno v:
Journal of Pediatric Surgery Case Reports, Vol 101, Iss , Pp 102760- (2024)
Introduction: Children with 45X/46XY difference/disorder of sex development (DSD) have varying internal/external genitalia/gonads, Turner-like features, and increased risk of gonadal malignancy. We present a case of concomitant virilization and femin
Externí odkaz:
https://doaj.org/article/3cb6af2929534bd89c6fb16eeb6b77e9