WELCOME TO THE HYPOHH HOME PAGE



Updated web site.



A new Kallmann syndrome website has been created and is now on line. Over the next few months all the content from this website will be updated and transferred to the new website.

It is hoped that the new web site will be a good source of information on Kallmann syndrome and related conditions. The new web site also contains a e-mail forum and links to other Kallmann sites to be found on the internet.

The site can be found at www.kallmanns.org or by clicking the following link.

Kallmann's syndrome web site


July 2008.



USA Kallmann Syndrome Meeting 2008.



As a result of the meeting held in the UK it is proposed that a similar meeting is to be held in the USA in 2008.

It will be held in Boston, Massachusetts on October 24th-25th 2008.

The provisional plan is for a meet and greet Friday evening, probably at a hotel near the hospital and Saturday would be the main meeting at Massachusetts General Hospital all day.

Boston General is a world leading centre in research for the genetic causes and treatment of KS / HH. Staff from the hospital including Dr Nelly Pitteloud will be speakers at the meeting.

Web site for information on Dr Pitteloud's work at Boston.

Visitor's information for Boston General Hospital.

The meeting is a good chance for people with KS / HH to meet other people with this rare condition. It is both a social event and a chance to meet specialist doctors and to learn more about the condition and any up to date treatments available.

For more information please e-mail:
kallmann-syndrome@hotmail.co.uk

UK Kallmann Syndrome Meeting 2008.



A meeting is being held in the UK for people with Kallmann Syndrome and HH. It is mainly a social event, a chance for people with this rare condition to meet other people with the same condition.

There will also be short presentations from a couple of specialists in Kallmann Syndrome on the current aspects of diagnosis and treatments available. They will then be available to answer any questions raised.

The meeting is to be held in Worcester on the 12th April 2008.

Confirmed guest speakers are:

Professor Pierre Bouloux. Royal Free Hospital, London.

Dr Nelly Pitteloud. Massachusetts General Hospital, Boston, USA.

For more information please e-mail:
kallmann-syndrome@hotmail.co.uk


Travel directions - click here.




HYPOHH.net is the official web site for HYPOHH, the patient support organisation for people with one of a specific group of rare hormonal diseases called hypogonadotrophic hypogonadism.

Hypogonadotrophic hypogonadism is characterised by a failure to go through or to complete puberty naturally and can affect both men and women. In most cases, hypogonadotrophic hypogonadism can be successfully treated by means of specialised hormone replacement therapy.

Without treatment people with this condition will very likely be infertile and have an increased risk of developing osteoporosis or 'brittle bones'. With the correct diagnosis and treatment, fertility can be achieved in many cases and the risk of osteoporosis reduced.

One form of hypogonadotrophic hypogonadism (HH) is known as Kallmann syndrome which has the additional characteristic of an absent or abnormally low sense of smell. There are a range of conditions that fall under the category of HH and it is important to receive specialist medical advice so that the correct diagnosis can be reached and appropriate treatment given.

Kallmann syndrome and other related HH conditions are congenital conditions and as such are present from birth. However the genetic basis of these conditions is not fully understood. Kallmann syndrome and HH can be inherited through the generations but it is sometimes very difficult for doctors to predict if this will occur.

HYPOHH.net is designed to provide with as much to up to date information as possible and to direct you to other sites where information and help is available.



LATEST NEWS. - click here



Here is a link to a discussion forum set up by a Kallmann Syndrome patient. The message board will allow people to get in contact with each other and ask any questions they may have, on any topic they wish.

Kallmann Syndrome Forum - click here.



What is hypogonadism ? - click here.




Here is a link to some Frequently Asked Questions on Kallmann Syndrome and other forms of HH. There is other information available on the listed websites, including current medical papers and research. There is a news section on the Kallmanns.org web site where any current news stories are posted in addition to information on this website.

Kallmann's FAQ - click here



My new web blog





There are two web based e-mail discussion forums for people with Kallmann's or HH. Both contain members from around the world. One is hosted by MSN the other by Yahoo.

Both groups contain members from around the world. There are members there who would be happy to answer any questions or just to have a discussion on any matter with people with the same condition. Both sites have a files and database section where you can get more information. Both sites are good way of getting in touch with other people with the same condition, and for families and friends to get more information.

Yahoo Group - Kallmann's syndrome.

Group on MSN - Men with Kallmann's syndrome.



Fertility Treatments



Hormone Replacement Treatments



Medical Papers



Genetics & Inheritance



Methods of Diagnosis



Osteoporosis Information



Psychological & Practical Issues



 

 


Happy surfing !