MedlinePlus Medical Encyclopedia: Hypogonadotropic hypogonadism

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Hypogonadotropic hypogonadism

Contents of this page:
Illustrations Alternative Names Definition Causes Symptoms Exams and Tests	Treatment Outlook (Prognosis) Possible Complications When to Contact a Medical Professional Prevention References

Illustrations

Endocrine glands

The pituitary gland

Pituitary hormones

Alternative Names Return to top

Gonadotropin deficiency; Secondary hypogonadism; Kallmann syndrome

Definition Return to top

Hypogonadotropic hypogonadism is absent or decreased function of the male testes or the female ovaries. It is considered a form of secondary hypogonadism, which means the condition is due to a problem with the pituitary or hypothalamus gland.

See also: Hypogonadism

Causes Return to top

Hypogonadotropic hypogonadism results from the absence of the gonadal stimulating pituitary hormones: Follicle stimulating hormone (FSH) and Luteinizing hormone (LH).

Normally, the hypothalamus in the brain releases gonadotropin-releasing hormone (GnRH), which stimulates the pituitary gland to release other hormones, including FSH and LH. These hormones tell the female ovaries and male testes to secrete hormones that are responsible for normal sexual development in puberty. A disruption in this chain of events causes a deficiency of the sex hormones and halts normal sexual maturation.

Failure of the hypothalamus is most commonly a result of Kallmann syndrome. Kallmann syndrome is an inherited form of hypogonadotropic hypogonadism that usually includes involves a disorder with the sense of smell.

Symptoms Return to top

Absence of secondary sexual characteristics such as pubic, facial, and underarm hair
Inability to smell (in some cases)
Lack of development at puberty (may involve incomplete development or a significant delay in development)
Underdeveloped testicles
Short stature (in some cases)

Exams and Tests Return to top

Tests that may be done include:

Blood tests to measure various hormone levels
LH response to GnRH
MRI of the head

Treatment Return to top

Treatment depends on the source of the problem but may involve:

Injections of testosterone
Slow-release testosterone skin patch
Estrogen and progesterone pills
GnRH injections

Outlook (Prognosis) Return to top

With proper hormonal stimulation, puberty can occur and fertility may be restored.

Possible Complications Return to top

Delayed puberty
Infertility
Low self-esteem due to late onset of puberty; emotional support may be helpful

When to Contact a Medical Professional Return to top

Call your health care provider if your child does not enter puberty as expected.

Prevention Return to top

Prevention depends on the cause. Genetic counseling may be appropriate for individuals with a family history of inherited disorders associated with hypogonadism. Prevention of serious head injuries reduces the risk of pituitary injury associated hypogonadotropic hypogonadism.

References Return to top

AACE Thyroid Task Force. AACE Hypogonadism Guidelines. Endocr Pract. 2002;8(6) 441.

Update Date: 10/24/2007

Updated by: Robert Hurd, MD, Professor of Endocrinology, Department of Biology, Xavier University, Cincinnati, OH, and physician in the Primary Care Clinic, Cincinnati Veterans Administration Medical Center, Cincinnati, Ohio. Review provided by VeriMed Healthcare Network.

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