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A boy is diagnosed with a rare congenital Kallmann syndrome. This syndrome is ch...
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A boy is diagnosed with a rare congenital Kallmann syndrome. This syndrome is characterized by anosmia (absence of smell) and reduced or zero production of the gonadotropin-releasing hormone GnRH, which leads to reduced production of the follicle-stimulating hormone FSH and luteinizing hormone LH, and subsequently to delayed or no puberty (pubertas tarda). Which cells are the normal source of FSH and LH?
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