A Study to Characterize Epidemiology, Clinical and Genetic Features of Kallmann Syndrome in Finland

Kallmann Syndrome in Finland

Objective is to characterize epidemiology, clinical and genetic features of Kallmann syndrome in Finland.

Kallmann syndrome is comprised of idiopathic hypogonadotropic hypogonadism and anosmia (inability to smell). Associated phenotypes may include cryptorchidism, microphallus, bone deformations, mirror movements, hearing loss and infertility. Objective is to characterize epidemiology, clinical and genetic features of Kallmann syndrome in Finland.

Inclusion Criteria:

• Kallmann syndrome
• Age 15 yrs or more

Exclusion Criteria:

• Severe mental retardation