Hypergonadotropic hypogonadism: Difference between revisions
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{{Infobox medical condition | |||
| name = Hypergonadotropic hypogonadism | |||
{{ | | synonyms = Primary hypogonadism | ||
| image = | |||
| caption = | |||
| field = [[Endocrinology]] | |||
}} | |||
'''Hypergonadotropic hypogonadism''' (HH), also known as primary hypogonadism, is a condition characterized by the reduced function of the [[gonads]] (the [[ovary|ovaries]] in females and [[testis|testes]] in males), with a consequent decrease in the production of [[sex hormones]]. This reduction in hormone levels leads to various clinical symptoms depending on the age at onset and the degree of hormone deficiency. | |||
==Causes== | |||
Hypergonadotropic hypogonadism is primarily caused by an intrinsic problem with the gonads. This can be due to: | |||
* [[Genetic disorders]], such as [[Turner syndrome]] in females and [[Klinefelter syndrome]] in males. | |||
* Damage to the gonads from infections like [[mumps]], trauma, or radiation. | |||
* Autoimmune disorders targeting the gonadal tissues. | |||
* [[Chemotherapy]] or radiation therapy that affects gonadal function. | |||
==Pathophysiology== | |||
In hypergonadotropic hypogonadism, the levels of [[gonadotropins]] ([[Follicle-stimulating hormone|FSH]] and [[Luteinizing hormone|LH]]) are elevated. This is because the pituitary gland produces more FSH and LH in response to the low levels of sex hormones. The increased levels of gonadotropins are unable to stimulate the dysfunctional gonads to produce hormones, leading to a state of hypogonadism. | |||
==Symptoms== | |||
The symptoms of hypergonadotropic hypogonadism vary based on the age of onset: | |||
* In children, it can lead to [[delayed puberty]] and may manifest as a failure to develop secondary sexual characteristics. | |||
* In adults, symptoms may include decreased libido, [[erectile dysfunction]], infertility, fatigue, hot flashes, and osteoporosis. | |||
==Diagnosis== | |||
Diagnosis of hypergonadotropic hypogonadism involves: | |||
* Clinical assessment of sexual development and symptoms. | |||
* Blood tests showing elevated levels of FSH and LH. | |||
* Low levels of sex hormones (estrogen in females and testosterone in males). | |||
* Imaging studies like ultrasound or MRI may be used to assess the physical structure of the gonads. | |||
==Treatment== | |||
Treatment focuses on hormone replacement therapy to manage symptoms and prevent complications: | |||
* [[Testosterone]] replacement therapy for males. | |||
* Estrogen and progesterone therapy for females. | |||
* Monitoring for potential side effects of long-term hormone therapy, such as cardiovascular risks and bone health. | |||
==Prognosis== | |||
With appropriate management, individuals with hypergonadotropic hypogonadism can lead relatively normal lives, although they often require lifelong hormone therapy and monitoring for associated health issues. | |||
==See also== | |||
* [[Hypogonadism]] | |||
* [[Hypothalamic disease]] | |||
* [[Pituitary disorders]] | |||
[[Category:Endocrine diseases]] | |||
[[Category:Reproductive system]] | |||
{{medicine-stub}} | |||
Latest revision as of 20:23, 7 August 2024
| Hypergonadotropic hypogonadism | |
|---|---|
| Synonyms | Primary hypogonadism |
| Pronounce | N/A |
| Specialty | N/A |
| Symptoms | N/A |
| Complications | N/A |
| Onset | N/A |
| Duration | N/A |
| Types | N/A |
| Causes | N/A |
| Risks | N/A |
| Diagnosis | N/A |
| Differential diagnosis | N/A |
| Prevention | N/A |
| Treatment | N/A |
| Medication | N/A |
| Prognosis | N/A |
| Frequency | N/A |
| Deaths | N/A |
Hypergonadotropic hypogonadism (HH), also known as primary hypogonadism, is a condition characterized by the reduced function of the gonads (the ovaries in females and testes in males), with a consequent decrease in the production of sex hormones. This reduction in hormone levels leads to various clinical symptoms depending on the age at onset and the degree of hormone deficiency.
Causes[edit]
Hypergonadotropic hypogonadism is primarily caused by an intrinsic problem with the gonads. This can be due to:
- Genetic disorders, such as Turner syndrome in females and Klinefelter syndrome in males.
- Damage to the gonads from infections like mumps, trauma, or radiation.
- Autoimmune disorders targeting the gonadal tissues.
- Chemotherapy or radiation therapy that affects gonadal function.
Pathophysiology[edit]
In hypergonadotropic hypogonadism, the levels of gonadotropins (FSH and LH) are elevated. This is because the pituitary gland produces more FSH and LH in response to the low levels of sex hormones. The increased levels of gonadotropins are unable to stimulate the dysfunctional gonads to produce hormones, leading to a state of hypogonadism.
Symptoms[edit]
The symptoms of hypergonadotropic hypogonadism vary based on the age of onset:
- In children, it can lead to delayed puberty and may manifest as a failure to develop secondary sexual characteristics.
- In adults, symptoms may include decreased libido, erectile dysfunction, infertility, fatigue, hot flashes, and osteoporosis.
Diagnosis[edit]
Diagnosis of hypergonadotropic hypogonadism involves:
- Clinical assessment of sexual development and symptoms.
- Blood tests showing elevated levels of FSH and LH.
- Low levels of sex hormones (estrogen in females and testosterone in males).
- Imaging studies like ultrasound or MRI may be used to assess the physical structure of the gonads.
Treatment[edit]
Treatment focuses on hormone replacement therapy to manage symptoms and prevent complications:
- Testosterone replacement therapy for males.
- Estrogen and progesterone therapy for females.
- Monitoring for potential side effects of long-term hormone therapy, such as cardiovascular risks and bone health.
Prognosis[edit]
With appropriate management, individuals with hypergonadotropic hypogonadism can lead relatively normal lives, although they often require lifelong hormone therapy and monitoring for associated health issues.
See also[edit]
