- General questions
- What is the best age for treatment to start ?
- Questions to ask the GP if you are worried about delayed puberty:
- What is Kallmann's syndrome? (1)
- When was Kallmann's syndrome first discovered?
- When does puberty become ‘delayed’?
- What does hypogonadal mean?
- What does hypogonadotrophic mean?
- What does congenital mean?
- What is the genetic basis of KS and IHH ?
- Why is testosterone important?
- Are there any famous people known to have Kallmann's syndrome ?
- FAQ's
- Diagnosis
- Treatment Options
- Fertility Options
- Osteoporosis Risks
- Medical Papers
- Genetics and Inheritance
- External web sites
Kallmann's Syndrome Information
Navigation
User login
Medical Warning
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.
Search
Site Counter
- Site Counter: 310238Unique Visitor: 46658Registered Users: 1217Unregistered Users: 17Published Nodes: 176Unpublished Nodes: 0Your IP: 38.107.191.116Since: 2008-06-29
© 2008 Neil Smith
When was Kallmann's syndrome first discovered?
Kallmann's syndrome is named after the German born, 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.
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.

