Results 111 to 120 of about 278,652 (177)

Role of Loss of mRNA-7a2 in Congenital Hypogonadotropic Hypogonadism and Male Infertility

Journal of Health and Rehabilitation Research
Background: Congenital Hypogonadotropic Hypogonadism (CHH) is a condition characterized by deficient secretion of gonadotropin-releasing hormone (GnRH), leading to impaired reproductive function and male infertility.
Tehmina Talib, Shaista Jabeen, Hamra Bano, Uroosa Aslam, Iqra Mukhtar, Fizah Rubab, Bushra Parveen, Sajal Batool, U. Khalid, Najma Badar, Rabea Ejaz   +10 more
semanticscholar   +1 more source

A bibliometric analysis of Kallmann syndrome: trends, hotspots, and future directions

Orphanet Journal of Rare Diseases
Background Kallmann syndrome (KS) is a rare congenital disorder characterized by hypogonadotropic hypogonadism secondary to deficient gonadotropin-releasing hormone (GnRH) secretion, often accompanied by partial or complete anosmia.
Hailei Han, Bin Ma, Jinmi Liu, Donglin Chai, Qinghua Sun, Ruiqing Zhang, Yanqing Guo   +6 more
doaj   +1 more source

(350) EFFICACY AND PREDICTORS OF SPERMATOGENESIS INDUCTION UPON GONADOTROPIN AND GNRH THERAPY IN CONGENITAL HYPOGONADOTROPIC HYPOGONADISM: A META-ANALYSIS

Journal of Sexual Medicine
Congenital Hypogonadotropic Hypogonadism (CHH) is among the few causes of male infertility, which could benefit from a rationale treatment. Both gonadotropin and GnRH therapy proved effective in inducing spermatogenesis in patients with CHH ...
Dimitri Yannas, L. Vignozzi, Giovanni Corona, M. Maggi, G. Rastrelli   +4 more
semanticscholar   +1 more source

MRI of ectopic posterior pituitary gland with dysgenesis of pituitary stalk in a patient with hypogonadotropic hypogonadism

, 2018
The ectopic posterior pituitary is a rare condition which is characterized by the ectopic location of posterior lobe of pituitary, pituitary stalk abnormalities, and associated clinical manifestations of anterior lobe related growth hormone dysfunction ...
Ramanivas Sundareyan, David Jenkins, Anjumara Nilak, Ashim Kumar Lahiri   +3 more
core   +1 more source

Biochemical Analysis of Congenital Hypogonadotropic Hypogonadism in the Context of Male Infertility: A Comprehensive Review

Journal of Health and Rehabilitation Research
Background: Male infertility encompasses various etiologies, with Congenital Hypogonadotropic Hypogonadism (CHH) standing out as a significant factor. CHH arises from multiple systems, including genetic abnormalities and hormonal imbalances that impair ...
Tehmina, Laila Siraj, Mahnoor Arif, Layiba Rameen, Husna Anwar, Uroosa Aslam, Hania Ibrar, Shazia Shamas   +7 more
semanticscholar   +1 more source

Comorbidity of schizophrenia and Kallmann’s Syndrome: a case report [PDF]

Düşünen Adam Psikiyatri ve Nörolojik Bilimler Dergisi, 2011
Kallmann’s Syndrome (KS) is a genetic disorder characterized by hypogonadotropic hypogonadism accompanied by anosmia or hyposmia. In addition, various abnormalities may be seen including anomalies in skeletal system, abnormal eye movements, congenital ...
Bahadir Bakim, Ersin Turkyilmaz, Oguz Karamustafalioglu, Onur Tankaya, Burcu Goksan Yavuz   +4 more
doaj  

Gonadotropins in hypogonadotropic hypogonadism in adolescents: prospects of treatment

, 2021
Analytical review of modern technologies of hypogonadotropic hypogonadism therapy in adolescents was presented, using recombinant gonadotropins, currently recognized as an effective remedy of puberty induction and substitutive hormone therapy in the ...
I. Yu. Ioffe, L. A. Zhelenina, Yu. L. Skorodok, I. L. Nikitina   +3 more
core  

Nasal reconstruction in a rare case of unilateral arhinia in bosma arhinia microphthalmia syndrome

Turkish Journal of Plastic Surgery
Bosma arhinia microphthalmia (BAM) is a very rare illness, with fewer than 100 cases documented worldwide. Criteria for diagnosis of BAM syndrome include congenital absence of nose (arhinia) or hypoplasia, hypogonadotropic hypogonadism, and eye defects ...
Kapil S Agrawal, Armaan Khosa, Vidhi Mehta, Vinita Puri   +3 more
doaj   +1 more source

Additional file 1: of Growth and descent of the testes in infants with hypogonadotropic hypogonadism receiving subcutaneous gonadotropin infusion

, 2016
Specific bibliography of orchiopexy in hypogonadotropic hypogonadism patients. (DOCX 147 ...
Pierre Bougneres (3510563), Anne-Sophie Lambert (3510560)   +1 more
core   +1 more source

Digenic CHD7 and SMCHD1 inheritance Unveils phenotypic variability in a family mainly presenting with hypogonadotropic hypogonadism

Heliyon
Objectives: CHARGE syndrome is a congenital hereditary condition involving multiple systems. Patients are easily misdiagnosed with idiopathic hypogonadotropic hypogonadism (IHH) due to the overlap of clinical manifestations.
Tian Wang, Wu Ren, Fangfang Fu, Hairong Wang, Yan Li, Jie Duan   +5 more
doaj   +1 more source