Results 91 to 100 of about 23,463 (198)
Objective: To evaluate the differences in thyroid volume and thyroid functions between male patients newly diagnosed with idiopathic hypogonadotropic hypogonadism (IHH) and healthy ...
Barker, Dilek +6 more
core
Hypopituitarism masquerading as Prasad's syndrome: a case report
Prasad's syndrome is characterized by geophagia, growth retardation, hypogonadism, and zinc deficiency. We report a 15-year-old boy whose medical history and clinical and laboratory findings were fully compatible with Prasad's syndrome.
Fatma Demirel +5 more
doaj
Two consanguineous Qatari siblings presented for evaluation: a 17-4/12-year-old male with hypogonadotropic hypogonadism, alopecia, intellectual disability, and microcephaly and his 19-year-old sister with primary amenorrhea, alopecia, and normal ...
Molly B. Sheridan +4 more
doaj +1 more source
Supplemental Materials for “Differential contributions of common genetic variants to constitutional delay of puberty and idiopathic hypogonadotropic hypogonadism”
Yee-Ming Chan (8287836) +1 more
core +1 more source
Heart failure and hypogonadotropic hypogonadism are the most frequent clinical problems encountered in patients with juvenile idiopathic hemochromatosis (JIH).
G Farina +6 more
doaj
Bone Mineral Density in Adolescent Girls with Hypogonadotropic and Hypergonadotropic Hypogonadism
Objective: Deficiency of sex steroids has a negative impact on bone mineral content. In studies conducted on postmenopausal women and animal studies, elevated follicle-stimulating hormone (FSH) levels were found to be correlated with a decrease in bone ...
Baran, Rıza Taner +4 more
core +1 more source
"The significance of the GNRH 1 gene polymorphism (rs 6185, rs1812594) in the development of idiopathic hypogonadotropic hypogonadism." [PDF]
The purpose of the study is to study the significance of the GNRH 1 gene polymorphism (rs 6185, rs1812594) in the development of idiopathic hypogonadotropic hypogonadism in boys and ...
Mavlonov U.Kh +3 more
core +1 more source
Update on the Genetics of Idiopathic Hypogonadotropic Hypogonadism
Traditionally, idiopathic hypogonadotropic hypogonadism (IHH) is divided into two major categories: Kallmann syndrome (KS) and normosmic IHH (nIHH). To date, inactivating variants in more than 50 genes have been reported to cause IHH. These mutations are estimated to account for up to 50% of all apparently hereditary cases.
openaire +4 more sources
The objective of this study was to evaluate the gonadal function in men with type 2 diabetes with erectile dysfunction. We examine records of 50 patients with type 2 diabetes and erectile dysfunction who had low free testosterone concentrations.
Khaishagi, Assad +5 more
core +1 more source
Epidemiology, diagnosis, and treatment of male hypogonadotropic hypogonadism
Hypogonadotropic hypogonadism (HH), or secondary hypogonadism, is a clinical condition due to an impairment of the pituitary function, characterized by low testosterone plasma levels associated with normal or low FSH and LH plasma levels.
C. Krausz +68 more
core +1 more source

