Normosmic congenital hypogonadotropic hypogonadism (Q106516): Difference between revisions
From determinar.ia.br - Determine suas informações
Changed an Item |
Changed an Item |
||
| Property / Canary Token | |||
dki-india-ID_1675702254 | |||
| Property / Canary Token: dki-india-ID_1675702254 / rank | |||
Normal rank | |||
Revision as of 13:30, 17 August 2026
This is a normosmic congenital condition which is characterised by hypogonadism due to an impaired secretion of gonadotropins, including follicle-stimulating hormone (FSH) and luteinizing hormone (LH), by the pituitary gland in the brain, and in turn decreased gonadotropin levels and a resultant lack of sex steroid production.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1675702254 |
||
| English | Normosmic congenital hypogonadotropic hypogonadism |
This is a normosmic congenital condition which is characterised by hypogonadism due to an impaired secretion of gonadotropins, including follicle-stimulating hormone (FSH) and luteinizing hormone (LH), by the pituitary gland in the brain, and in turn decreased gonadotropin levels and a resultant lack of sex steroid production. |
Statements
CID11:ID_1675702254
0 references
dki-india-ID_1675702254
0 references
