Leydig cell hypoplasia (Q91113): Difference between revisions
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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 e outros hormônios sexuais andrógenos. | |||
| 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 testosterone and other androgen sex hormones | |||
Revision as of 18:06, 15 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 testosterone and other androgen sex hormones
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_472787488 |
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| English | Leydig cell hypoplasia |
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 testosterone and other androgen sex hormones |
