Kallmann's Syndrome Information
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Information on this site is provided by people with personal experience of Kallmann's syndrome. Symptoms and appropriate treatments are different for different people. You should not treat anything on this site as a substitute for advice from a trained medical professional.
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Kallmann's syndrome & sense of smell.
Kallmann's syndrome has one key symptom that sets it apart from other forms of hypogonadotrophic hypogonadism; the lack of sense of smell.
The absence of the sense of smell (anosmia), or a vastly reduced sense of smell (hyposmia) could act as marker that can lead to a diagnosis of Kallmann’s syndrome. Reduced sense of smell can happen on its own for a number of other reasons but in conjunction with delayed puberty might lead a doctor to suspect a case of Kallmann’s syndrome.
The sense of smell can easily be tested for by a combination of two simple tests.
One is a basic alcohol smell taste which uses different concentrations of the same smell, normally alcohol, to detect the threshold at which the smell is detected.
The other test is a more involved test involving a range of different smells to see which can be identified correctly.
A commonly used test is the University of Pennsylvania Smell Identification Test (UPSIT).
This involves a scoring method on the above tests and gives a score of between 0 and 100.
A perfect score would be 100.
0–10 is considered anosmia.
10–40 severely hyposmic.
40–60 moderately hyposmic.
60–90 mildly hyposmic.
90–100 is considered normal.

