LH resistance due to complete LH receptor inactivation (Q104184): Difference between revisions

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Latest revision as of 10:03, 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 complete LH receptor inactivation.

Language	Label	Description	Also known as
default for all languages	ID_232167901
English	LH resistance due to complete 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 complete LH receptor inactivation.