LH resistance due to partial LH receptor inactivation (Q104178): Difference between revisions
From determinar.ia.br - Determine suas informações
Created a new Item |
Changed label, description and/or aliases in pt-br, en |
||
| description / pt-br | description / pt-br | ||
Síndrome endócrina e genética autossômica recessiva rara, caracterizada por uma incapacidade do corpo de responder ao hormônio luteinizante (LH), uma gonadotrofina que normalmente é responsável por sinalizar às células de Leydig dos testículos para que produzam testosterona. Esse diagnóstico se deve à inativação parcial do receptor de LH. | |||
| description / en | description / en | ||
This is a rare autosomal recessive genetic and endocrine syndrome, characterised by an inability of the body to respond to luteinizing hormone (LH), a gonadotropin which is normally responsible for signalling Leydig cells of the testicles to produce testos. This diagnosis is due to partial LH receptor inactivation. | |||
Revision as of 10:02, 17 August 2026
This is a rare autosomal recessive genetic and endocrine syndrome, characterised by an inability of the body to respond to luteinizing hormone (LH), a gonadotropin which is normally responsible for signalling Leydig cells of the testicles to produce testos. This diagnosis is due to partial LH receptor inactivation.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_74297048 |
||
| English | LH resistance due to partial LH receptor inactivation |
This is a rare autosomal recessive genetic and endocrine syndrome, characterised by an inability of the body to respond to luteinizing hormone (LH), a gonadotropin which is normally responsible for signalling Leydig cells of the testicles to produce testos. This diagnosis is due to partial LH receptor inactivation. |
