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This is a rare autosomal recessive genetic and endocrine syndrome, characterised by a complete inability of the body to respond to luteinising hormone (LH), a gonadotropin which is normally responsible for signalling Leydig cells of the testicles to produce testosterone.
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This is a rare autosomal recessive genetic and endocrine syndrome, characterized by a complete 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.
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