Hypogonadotropic Hypogonadism

What is Hypogonadotropic Hypogonadism?

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

Alternative names

Gonadotropin deficiency; Secondary hypogonadism; Kallmann syndrome

Causes

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 involves a disorder with the sense of smell.

Symptoms & Signs

• 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

Tests that may be done include:

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

Treatments

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

Prognosis

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

Possible Complications

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

When to contact a medical professional

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

Prevention

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

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

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Review Date: 10/24/2007

Reviewed 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.