Kallmann syndrome is a condition that’s characterized by absent or delayed puberty and a lack or loss of sense of smell. Kallmann syndrome may be accompanied by other symptoms, including hearing loss and cleft palate. The condition is typically treated with hormone replacement therapy.
4 things you should know about Kallmann syndrome
- Kallmann syndrome is a congenital condition, which means people are born with it. Statistically, the condition occurs in 1 out of every 30,000 males and 1 out of every 120,000 females.
- Research indicates that gene mutations associated with Kallmann syndrome affect olfactory (sense of smell) nerve cells in your brain. As a result, your sense of smell is impaired.
- No development of sex characteristics in males at puberty, such as enlarged penis and testes, facial hair and deepening of their voice can cause Kallmann syndrome
- There’s currently no known cure for Kallmann syndrome. However, continued research is being performed in this area.
And finally, If your child hasn’t started showing signs of puberty around the same time as their peers, then it’s a good idea to schedule a visit with their healthcare provider. They can run the appropriate tests and talk with you about treatment options. These informations are gotten from cleaveland clinics.
Leave a Reply