Kallmann Syndome

Kallmann syndrome is a rare genetic hormonal condition that is characterized by a failure to start or a failure to complete puberty. It is also accompanied by a lack of sense of smell (anosmia) or a highly reduced sense of smell (hyposmia). The condition can occur in both males and females but is more commonly diagnosed in males. Left untreated, patients with Kallmann syndrome will almost invariably be infertile. Kallmann syndrome is a form of hypogonadotropic hypogonadism (HH).

Test Details
Description:
Delivery Time:
10 days
Sample:
2-5 Ml Venous Blood Sample / DNA sample
Alternative:

Kallmann syndrome is a rare genetic hormonal condition that is characterized by a failure to start or a failure to complete puberty. It is also accompanied by a lack of sense of smell (anosmia) or a highly reduced sense of smell (hyposmia). The condition can occur in both males and females but is more commonly diagnosed in males. Left untreated, patients with Kallmann syndrome will almost invariably be infertile. Kallmann syndrome is a form of hypogonadotropic hypogonadism (HH).

Test Details
Description:
Multiplex ligation-dependent probe amplification
Delivery Time:
10 days
Sample:
2-5 mL Blood - Lavender Top Tube
Alternative:
Description:
Delivery Time:
10 days
Sample:
6 ml. blood sampling
Alternative: