Kallmann syndrome

Outwardly there is nothing striking about a person with Kallmann syndrome.

Another aspect of Kallmann syndrome is the social isolation.

Since it is such a rare condition a lot of patients with Kallmann syndrome have never even met or talked to a fellow patient.

Having Kallmann syndrome can have a profound effect on a person's life, however it will affect different people in different ways.

There are three forms of Kallmann syndrome.

Kallmann syndrome and hypogonadotropic hypogonadism do not exist as distinct conditions.

He is credited as being one of the first scientists to recognize the disorder known as Kallmann syndrome.

Kallmann syndrome is also associated with a lack of sense of smell (anosmia).

The third and most rare form of Kallmann syndrome is KAL3.

Clinically, mutation results in the X-linked form of Kallmann syndrome.

Lifelong hyposmia could be caused by Kallmann syndrome.

Kallmann syndrome and other forms of HH affect both men and women.

Important It is possible that the main title of the report Kallmann Syndrome is not the name you expected.

Kallmann syndrome is a genetic condition which results in the failure to commence or the non-completion of puberty.

Once treatment is started and normal hormone levels are restored there are no side effects or life expectancy issues associated with having Kallmann syndrome.

Reduced sense of smell (hyposmia) suggests Kallmann syndrome.

Provides support, information and encouragement to patients with Kallmann syndrome and other forms of hypogonadotrophic hypogonadism.

In women, late-onset Kallmann Syndrome can result in secondary amenorrhea.

This may also occur in other conditions, for example following trauma, in Kallmann syndrome or Parkinson's disease.

The best-known person who has Kallmann syndrome is the jazz vocalist Jimmy Scott.

The patients that cope better with Kallmann syndrome on the whole are those that are diagnosed before the age of 16 and have prompt treatment.

Examples of Hypothalamic defects include Kallmann syndrome.

Approximately 50% of HH cases occur with anosmia and can be termed as Kallmann syndrome.

Kallmann syndrome is recognized by anosmia due to mental retardation, hypogonadism, and the failure of the olfactory bulb to develop.

GnRH formation is congenitally absent in Kallmann syndrome.