Abstract
Kallmann's syndrome is characterized by hypogonadotropic hypogonadism and anosmia. Postmortem studies have revealed either hypoplasia or aplasia of the rhinencephalon, respectively, in patients with hyposmia and anosmia. This anatomical defect has now been demonstrated in vivo in four patients with Kallmann's syndrome by magnetic resonance imaging.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Adult
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Brain / pathology*
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Follicle Stimulating Hormone / blood
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Humans
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Hypogonadism / diagnosis*
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Hypothalamic Diseases / diagnosis*
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Luteinizing Hormone / blood
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Magnetic Resonance Spectroscopy*
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Male
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Olfaction Disorders / diagnosis*
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Testosterone / blood
Substances
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Testosterone
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Luteinizing Hormone
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Follicle Stimulating Hormone