Zobrazeno 1 - 10
of 7 371
pro vyhledávání: '"hypogonadotropic hypogonadism"'
Publikováno v:
Asian Journal of Andrology, Vol 26, Iss 4, Pp 426-432 (2024)
Fibroblast growth factor receptor 1 (FGFR1) mutations are associated with congenital hypogonadotropic hypogonadism (CHH) through inheritance or spontaneous occurrence. We detected FGFR1 mutations in a Chinese cohort of 210 CHH patients at Peking Unio
Externí odkaz:
https://doaj.org/article/f8e12e0c33064e8ea9f8759bc105d73e
Autor:
Paola Chiarello, Giuseppe Seminara, Sabrina Bossio, Valentina Rocca, Emma Colao, Rodolfo Iuliano, Antonio Aversa
Publikováno v:
Endocrines, Vol 5, Iss 3, Pp 334-340 (2024)
Adult-onset cases of idiopathic hypogonadotropic hypogonadism (IHH) are characterized by partial or normal puberty development until adolescence and by the impairment of the hypothalamic–pituitary–gonadal (HPG) axis in adulthood. WDR11 and DCC ge
Externí odkaz:
https://doaj.org/article/8d389e8779d446448707f71fd3fff4fd
Autor:
Yassine Zouaghi, Anbreen Mazhar Choudhary, Saba Irshad, Michela Adamo, Khaleeq ur Rehman, Ambrin Fatima, Mariam Shahid, Nida Najmi, Fernanda De Azevedo Correa, Imen Habibi, Alexia Boizot, Nicolas J. Niederländer, Muhammad Ansar, Federico Santoni, James Acierno, Nelly Pitteloud
Publikováno v:
BMC Genomics, Vol 25, Iss 1, Pp 1-9 (2024)
Abstract Background/Objectives This study aims to elucidate the genetic causes of congenital hypogonadotropic hypogonadism (CHH), a rare genetic disorder resulting in GnRH deficiency, in six families from Pakistan. Methods Eighteen DNA samples from s
Externí odkaz:
https://doaj.org/article/ccf74a0fcaad4147bb07e27344df98d0
Publikováno v:
Journal of Medical Case Reports, Vol 18, Iss 1, Pp 1-8 (2024)
Abstract Background Currently, there is a scarcity of cases and diagnostic data regarding ectopic adrenocortical adenomas, particularly in relation to their impact on gonadal function and localization diagnostic techniques. We report a typical case o
Externí odkaz:
https://doaj.org/article/a1546032e28341758672721e89ba4e60
Autor:
Ghali Bennani, Soukaina Zahri, Mohamed Khaldi, Ghali Benouna, Abdenasser Drighil, Rachida Habbal
Publikováno v:
The Egyptian Heart Journal, Vol 76, Iss 1, Pp 1-5 (2024)
Abstract Background Kallmann–Morsier syndrome is a rare disease characterized by the association of congenital gonadotropic deficiency and anosmia or hyposmia. The cardiac manifestations associated with this syndrome are little known. Through this
Externí odkaz:
https://doaj.org/article/ea72cbaacb19459cad20f5dc9a9f89a1
Autor:
Azlansyah Azlansyah, Cennikon Pakpahan, Hermansyah Hermansyah, Faisal Yusuf Ashari, Gustavo Santos Rainato, Kenley Nathanael, Maxwell Salvador Surya Atmaja
Publikováno v:
Biomolecular and Health Science Journal, Vol 7, Iss 1, Pp 75-79 (2024)
Kallmann syndrome is defined as the association of hypogonadotropic hypogonadism and anosmia or hyposmia caused by abnormal migration of olfactory axons and neurons producing gonadotropin-releasing hormone. It is a nonlife-threatening disease with re
Externí odkaz:
https://doaj.org/article/2ab8cdd97ff9449c85f9dcb4d1a5b920
Publikováno v:
JCRPE, Vol 16, Iss 1, Pp 91-94 (2024)
Congenital hypogonadotropic hypogonadism (CHH) is a rare genetic disorder, resulting from impaired production, secretion, or action of gonadotropin-releasing hormone (GnRH). Variants of the KISS1R gene can result in CHH. Herein we describe a Chinese
Externí odkaz:
https://doaj.org/article/8a513a88871b48d6a54c8d2817f53cb6
Akademický článek
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Akademický článek
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Autor:
Federica Barbagallo, David Bosoni, Valeria Perone, Laura Cucinella, Davide Dealberti, Rossella Cannarella, Aldo E. Calogero, Rossella E. Nappi
Publikováno v:
Frontiers in Endocrinology, Vol 15 (2024)
Functional hypothalamic amenorrhea (FHA) is a common cause of amenorrhea and chronic anovulation in adolescent girls and young women, diagnosed after excluding other organic causes. It is commonly associated with calorie restriction, excessive physic
Externí odkaz:
https://doaj.org/article/efedf97e487a44f5b79a7515287a12a0