Results 51 to 60 of about 278,652 (177)

A case of hypogonadtropic hypogonadism due to hypophysitis discovered by secondary male infertility

IJU Case Reports, 2023
Introduction The main causes of secondary male infertility are varicocele and aging. It is rarely caused by adult‐onset hypopituitarism. The onset of hypopituitarism is often due to brain tumors, trauma, surgery, or congenital disorders.
Masatoshi Konishi, Yoko Maegawa, Masaru Tani, Toshihisa Asakura, Yujiro Hayashi, Yoichi Kakuta, Koichi Tsutahara, Kazuhiko Komori, Tetsuya Takao   +8 more
doaj   +1 more source

Predictors of reproductive and non-reproductive outcomes of gonadotropin mediated pubertal induction in male patients with congenital hypogonadotropic hypogonadism (CHH) dataset

, 2022
Dataseta for Predictors of reproductive and non-reproductive outcomes of gonadotropin mediated pubertal induction in male patients with congenital hypogonadotropic hypogonadism (CHH) 10.1007/S40618-021-01556-
Duminuco, Paolo, Cangiano, Biagio, Bresesti, Chiara, Guizzardi, Fabiana, Persani, Luca, Federici, Silvia, Vezzoli, Valeria, Cotellessa, Ludovica, Goggi, Giovanni, Bonomi, Marco   +9 more
core   +1 more source

Genetic and phenotypic differences between sexes in congenital hypogonadotropic hopogonadism(CHH):large cohort analysis from a single tertiary Centre. DATASET

, 2022
Database of the paper Gender differences in congenital hypogonadotropic hypogonadism (CHH): an analysis in a large cohort of CHH patients and an insight in female genotype and ...
Amer, Myriam, Cangiano, Biagio, Persani, Luca, Federici, Silvia, Messetti, Dario, Hrvat, Faris, Vezzoli, Valeria, Munari, Elisabetta Veronica, Goggi, Giovanni, Bonomi, Marco   +9 more
core   +1 more source

Clinical approach to the male with delayed puberty [PDF]

Archives of Endocrinology and Metabolism
Disorders of pubertal onset and progression are a common cause for referral to paediatric endocrinologists, with delayed puberty in males being particularly frequent. Pubertal development depends on the hypothalamic-pituitary-testicular (HPT) axis, which
Rodolfo A. Rey, Romina P. Grinspon, Sebastián Castro   +2 more
doaj   +1 more source

Psychological Aspects of Congenital Hypogonadotropic Hypogonadism

Frontiers in Endocrinology, 2019
Congenital hypogonadotropic hypogonadism/Kallmann syndrome (CHH/KS) is a rare, treatable form of infertility. Like other rare disease patients, individuals with CHH/KS frequently experience feelings of isolation, shame, and alienation.
Andrew A. Dwyer, Andrew A. Dwyer, Neil Smith, Richard Quinton   +3 more
doaj   +1 more source

Delayed-onset adrenal hypoplasia congenita and hypogonadotropic hypogonadism caused by a novel mutation in

Journal of International Medical Research, 2020
In this study, we described a male who presented with delayed-onset adrenal hypoplasia congenita (AHC) and mild hypogonadotropic hypogonadism (HHG) without a relevant family history. A novel mutation in the DAX1 (dosage-sensitive sex reversal, congenital
Siyue Liu, Libin Yan, Xinrong Zhou, Chen Chen, Daowen Wang, Gang Yuan   +5 more
doaj   +1 more source

Pituitary imaging findings in pediatric patients with idiopathic hypogonadotropic hypogonadism

, 2023
Objective. Idiopathic hypogonadotropic hypogonadism in children is a disease leading to a puberty absence. Some hypothalamic and pituitary defects cause hypogonadotropic hypogonadism.
Toprak Nursen, Bitkin Eda Celebi, Karaman Serap, Karaman, Serap, Nursen Toprak, Serap Karaman, Toprak, N., Bitkin, Eda Celebi, Bitkin, E.C., Eda Celebi Bitkin, Toprak, Nurşen, Karaman, S.   +11 more
core   +1 more source

Polythelia associated with hypogonadotropic hypogonadism in young male: A case report [PDF]

, 2021
Polythelia is a congenital anomaly in which there is a third or more nipples. Although it is a relatively rare condition, it is frequently associated with other congenital malformations including the cardiovascular, urogenital, and skeletal systems.
Mustafa Abdelmonem Hegazy, Abdelmonem Awad Mustafa Hegazy, Khaled Hadhoud   +2 more
core   +1 more source

NDNF variants are rare in patients with congenital hypogonadotropic hypogonadism

Human Genome Variation, 2021
Although NDNF was recently reported as a novel causative gene for congenital hypogonadotropic hypogonadism (CHH), this conclusion has yet to be validated. In this study, we sequenced NDNF in 61 Japanese CHH patients.
Satoshi Tamaoka, Erina Suzuki, Atsushi Hattori, Tsutomu Ogata, Maki Fukami, Yuko Katoh-Fukui   +5 more
doaj   +1 more source

Constitutional delay of puberty versus congenital hypogonadotropic hypogonadism: genetics, management and updates [PDF]

, 2019
Delayed puberty (DP) affects approximately 2% of adolescents. In the vast majority of patients in both sexes, it is due to constitutional delay of growth and puberty (CDGP), a self-limited condition in which puberty starts later than usual but progresses
Miettinen, Päivi J., Raivio, Taneli
core   +1 more source