Leydig cell hypoplasia (Q91113): Difference between revisions
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Revision as of 18:07, 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 |
||
| 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 |
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CID11:ID_472787488
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dki-india-ID_472787488
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Concluído
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