- General questions
- FAQ's
- 1. My doctor told me I have Kallmann's syndrome. What does this mean ?
- 2. When was Kallmann's syndrome first discovered ?
- 3. What does an endocrinologist do?
- 4. I have heard of "hormones" before, but what are they ?
- 5. What and where are my hypothalamus and pituitary gland ?
- 6. What happens during normal puberty ?
- 7. As a teenager, I didn't go through puberty at all. Why ?
- 8. How good are my chances of becoming a parent ?
- 9. Why did my doctor ask me whether or not I had a sense of smell ?
- 10. Why don't I have a sense of smell ?
- 11. What has my absent sense of smell got to do with absent puberty ?
- 12. Others have said that I have long arms and legs. Can this be true ?
- 13. Will I develop 'brittle bone disease' ?
- 14. What other characteristics of Kallmann's syndrome are there ?
- 15. What is the difference between Kallmann syndrome and Klinefelter syndrome ?
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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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© 2008 Neil Smith
2. When was Kallmann's syndrome first discovered ?
Kallmann's syndrome is named after the New York geneticist and psychiatrist Franz J. Kallmann, who, in 1944, was the first to offer a genetic explanation for a medical condition he observed in some of his patients who happened to be both sexually immature and anosmic. Although some of his original observations and conclusions were to be questioned in later years as more was learned about the disease, his work was nevertheless an important and valuable milestone.
However, Kallmann was not the first to recognise a possible link between sexual immaturity and an absent sense of smell. Eighty years earlier, the Spanish doctor Aureliano Maestre de San Juan had carried out a post-mortem examination on a 40-year old man who had a small penis and very small testes. An interesting discovery was made. On examination of the dead man's brain, it was established that two small structures (the olfactory bulbs) were completely missing, a fact which explained his absent sense of smell (see answer to Question 10). A few years later, an Austrian medical journal published the findings of a Professor Heschl who made a similar discovery in a 45-year old man who also had small genitalia and little body and pubic hair. In 1914, the German doctor Franz Weidenreich suggested that there was a definite association between anosmia and a lack of sexual development and that consequently this represented a discrete syndrome. A syndrome is defined as a combination of signs and/or symptoms which causes a particular disease. In this case, the syndrome later became known as Kallmann's syndrome.
A lot has been learned about the disease since Kallmann's work in 1944. Thanks to advanced research techniques, it has been possible to identify the fundamental cause of the disease, to optimise forms of treatment and to explain how, in some cases, Kallmann's syndrome may be inherited. Much about Kallmann's syndrome is still not very well understood, but the pace at which medical research is currently revealing its secrets is considerable and hopefully, it will only be a matter of time before they are all revealed.

