Hypogonadism

Clinic

• Diminished functional activity of the gonads, that may result in diminished production of sex hormones.
• Hypoandrogenism (Low androgen e.g., testosterone) and Hypoestrogenism (Low estrogen e.g., estradiol)

• Hypogonadism, commonly referred to "low testosterone" and can also decrease other hormones including progesterone, DHEA, anti-Müllerian hormone, activin, and inhibin.
• Spermatogenesis and Ovulation may be impaired which causes complete infertility.
• Hypogonadism can involve just hormone production or just fertility, but most commonly involves both.
  • Examples of hypogonadism that affect hormone production more than fertility are hypopituitarism and Kallmann syndrome; in both cases, fertility is reduced until hormones are replaced but can be achieved solely with hormone replacement.
  • Examples of hypogonadism that affect fertility more than hormone production are Klinefelter syndrome and Kartagener syndrome.

Types

Primary hypogonadism

• Genetic: Klinefelter syndrome, Turner syndrome, Noonan syndrome, XY with SRY gene-immunity
• Acquired: MMP

LH and/or FSH are usually elevated, since the problem is in Testicles / Ovaries (Hyper-gonatropic hypogonadism)

Secondary hypogonadism

• Hypogonadotropic hypogonadism (HH) due to Hypopituitarism / Pituitary hypoplasia.
• Lack of hormone response is AIS (Androgen Insensitivity Syndrome)
• Isolated hypogonadotropic hypogonadism (IHH)= Idiopathic or congenital hypogonadotropic hypogonadism (CHH): HH due to deficiency in or insensitivity to GnRH where the function and anatomy of the anterior pituitary is normal and secondary causes of HH are not present
• In secondary hypogonadism, LH / FSH are normal or low, suggesting the problem is in the brain (Hypo-gonatropic hypogonadism
• Examples are
  • PCOS
  • Kallmann syndrome
  • Hemochromatosis
  • Diabetes mellitus

Central Hypogonadism

• Central hypogonadism referring to CNS / Hypothalamic defects including:
  • Genetic disorders such as Kallmann syndrome (Abnormal hypothalamic development)
  • Infections including HIV
  • Pituitary disorders
  • Inflammatory diseases including sarcoidosis, MTB and histiocytosis

Other

Hypogonadism can occur in other conditions, like Prader–Willi syndrome.

Signs / Symptoms

• Women: Amenorrhea, Decreased height+ Impaired Breast development Or Cessation of menstruation + Lowered libido + Loss of body hair + Hot flashes.
• Men: Impaired muscle + Impaired body hair development + Gynecomastia + Decreased height + Erectile dysfunction + Sexual difficulties.
• Central hypogonadism: Headaches + Impaired vision / Double vision + Milky discharge from the breast (Prolactin) + Symptoms caused by other hormone problems.

Hypogonadotrophic hypogonadism

• It is a subtype of hypogonadism
• Late, incomplete or lack of development at puberty
• Sometimes short stature or the inability to smell
• In females, a lack of breasts and menstrual periods, and in males a lack of sexual development, e.g., facial hair, penis and testes enlargement, deepening voice.