Anosmic congenital hypogonadotropic hypogonadism (Q106515): Difference between revisions
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Hipogonadismo hipogonadotrófico congênito anósmico (síndrome de Kallmann) é um transtorno congênito genético caracterizado pela associação de hipogonadismo hipogonadotrófico devido a deficiência de hormônio liberador de gonadotrofina (GnRH), e anosmia ou hiposmia (com hipoplasia ou aplasia de bulbo olfatório). | |||
| description / en | description / en | ||
Anosmic congenital hypogonadotropic hypogonadism (Kallmann syndrome) is a congenital genetic disorder characterised by the association of hypogonadotropic hypogonadism due to gonadotropin-releasing hormone (GnRH) deficiency, and anosmia or hyposmia (with hypoplasia or aplasia of the olfactory bulbs). | |||
Revision as of 13:30, 17 August 2026
Anosmic congenital hypogonadotropic hypogonadism (Kallmann syndrome) is a congenital genetic disorder characterised by the association of hypogonadotropic hypogonadism due to gonadotropin-releasing hormone (GnRH) deficiency, and anosmia or hyposmia (with hypoplasia or aplasia of the olfactory bulbs).
| Language | Label | Description | Also known as |
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| default for all languages | ID_1053735191 |
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| English | Anosmic congenital hypogonadotropic hypogonadism |
Anosmic congenital hypogonadotropic hypogonadism (Kallmann syndrome) is a congenital genetic disorder characterised by the association of hypogonadotropic hypogonadism due to gonadotropin-releasing hormone (GnRH) deficiency, and anosmia or hyposmia (with hypoplasia or aplasia of the olfactory bulbs). |
