Hypogonadism history and symptoms: Difference between revisions
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=== Common symptoms in female === | |||
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===Less common symptoms=== | ===Less common symptoms=== | ||
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Associate Editor(s)-in-Chief: Ahmed Elsaiey, MBBCH [2]
Overview
History and symptoms
History is important in diagnosis of hypogonadism in both males and females. The onset of the symptoms and previous congenital gonadal anomalies should be known.
- For both males and females:
- History is important to know if there was any gonadal abnormality since birth or not. The onset of puberty should also be known.
- Family history of delay of growth and development is also important.
- For males:
- History of any causes of testicular failure as radiation to testes, chemotherapy or drugs decreasing testosterone secretion.
- For females:
- Menstrual history is important and the date of menarche.
- History of increased androgen secretion as ance and hirsutism.
Common symptoms in males
Symptoms of hypogonadism depends on the onset of the disease whether before puberty or after. In this table, the common symptoms of hypogonadism in both periods are enlisted.[1][2]
| Pre-pubertal | Post-pubertal (Adult) |
|---|---|
Delayed puberty and loss of sexual characters:
|
|
Common symptoms in female
- Delayed puberty and loss of the secondary sexual characters:
Less common symptoms
- Headaches
- Visual loss
- Galactorrhea
- Anorexia nervosa
- Fatigue and weakness
- Loss of energy
- Depression
References
- ↑ Khera M, Broderick GA, Carson CC, Dobs AS, Faraday MM, Goldstein I; et al. (2016). "Adult-Onset Hypogonadism". Mayo Clin Proc. 91 (7): 908–26. doi:10.1016/j.mayocp.2016.04.022. PMID 27343020.
- ↑ Basaria S (2014). "Male hypogonadism". Lancet. 383 (9924): 1250–63. doi:10.1016/S0140-6736(13)61126-5. PMID 24119423.