Results 161 to 170 of about 23,463 (198)
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Gonadotropin Treatment for the Male Hypogonadotropic Hypogonadism
Current Pharmaceutical Design, 2021Hypogonadotropic hypogonadism (HH) is caused by a dysfunction in the hypothalamus and/or the pituitary gland and it can be congenital or acquired. This condition is biochemically characterized by low or inappropriately normal gonadotropin levels along with low total testosterone levels.
Luca Boeri +2 more
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Hypogonadotropic Hypogonadism from Osteopetrosis
Clinical Orthopaedics and Related Research, 1982A 47-year-old man with acquired hypogonadism of at least 15 years' duration was successfully treated with chorionic gonadotropin. Endocrine studies performed before and two months after discontinuation of gonadotropin therapy showed a decrease in serum testosterone level without secondary rise in serum gonadotropins.
J, Mazur, J, Wortsman
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Molecular causes of hypogonadotropic hypogonadism
Current Opinion in Obstetrics & Gynecology, 2010What controls puberty remains largely unknown and current gene mutations account for only about one-third of the apparently genetic cases of idiopathic hypogonadotropic hypogonadism. Lately important developments have occurred in this field.Substantial variation in clinical expression, from complete anosmia and hypogonadotropic hypogonadism to delayed ...
Ali Kemal, Topaloglu, Leman Damla, Kotan
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Reversal of Idiopathic Hypogonadotropic Hypogonadism
New England Journal of Medicine, 2007Idiopathic hypogonadotropic hypogonadism, which may be associated with anosmia (the Kallmann syndrome) or with a normal sense of smell, is a treatable form of male infertility caused by a congenital defect in the secretion or action of gonadotropin-releasing hormone (GnRH).
Raivio T +11 more
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Hypogonadotropic Hypogonadism with Anosmia
Andrologia, 2009Zusammenfassung Anhand von zwei eigenen Beobachtungen wird zum sog. Kallmann-Syndrom Stellung genommen. Es handelt sich dabei um einen hypogonadotropen Hypogonadismus beim Manne mit Anosmie. Verff. vertreten die Auffassung, das die exakte Diagnosestellung dieses Syndroms fur die Prognose auserordentlich bedeutsam ist, da man bei Pat.
Jan Peers, Omer Steeno, Pieter Moor
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Isolated Hypogonadotropic Hypogonadism With Syndactyly
Archives of Internal Medicine, 1984Although some skeletal malformations have been associated with hypogonadotropic hypogonadism, syndactyly, to our knowledge, has not. A 43-year-old man, with no family history of either condition, was identified as having isolated hypogonadotropic hypogonadism with syndactyly of the feet.
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Genetics of human hypogonadotropic hypogonadism
American Journal of Medical Genetics, 1999Humans with hypogonadotropic hypogonadism (HH) manifest irreversible pubertal delay, infertility, and low serum levels of follicle-stimulating hormone (FSH) and luteinizing hormone (LH). Although the genetic basis of this condition is largely unknown, mutations have been identified in approximately 5-10% of HH patients.
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Congenital Hypogonadotropic Hypogonadism
20151. Review the variable clinical presentation of men with CHH 2. Summarize what is known about the gene defects causing CHH 3.
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Management of congenital hypogonadotropic hypogonadism in females
Human Fertility, 2023Cheryl Fitzgerald
exaly
Isolated Hypogonadotropic Hypogonadism
Endocrine Abstracts, 2022Aung Nwe Ni, Jana Bujanova
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