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==Overview==
==Overview==
Hypogonadism may be classified according to the etiological site into three subtypes namely primary, secondary or combined. Hypogonadism can also be classified according to the age into two adult and child. Based on the causes, it can be classified into acquired or [[congenital]].<ref name="pmid23258624">{{cite journal| author=Rey RA, Grinspon RP, Gottlieb S, Pasqualini T, Knoblovits P, Aszpis S et al.| title=Male hypogonadism: an extended classification based on a developmental, endocrine physiology-based approach. | journal=Andrology | year= 2013 | volume= 1 | issue= 1 | pages= 3-16 | pmid=23258624 | doi=10.1111/j.2047-2927.2012.00008.x | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=23258624  }} </ref>
Hypogonadism may be classified according to the etiological site into three subtypes namely primary, secondary or combined. Hypogonadism can also be classified according to the age into two adult and child onset disease. Also, it could be classified based on the causes into [[acquired]] or [[congenital]].<ref name="pmid23258624">{{cite journal| author=Rey RA, Grinspon RP, Gottlieb S, Pasqualini T, Knoblovits P, Aszpis S et al.| title=Male hypogonadism: an extended classification based on a developmental, endocrine physiology-based approach. | journal=Andrology | year= 2013 | volume= 1 | issue= 1 | pages= 3-16 | pmid=23258624 | doi=10.1111/j.2047-2927.2012.00008.x | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=23258624  }} </ref>


==Classification==
==Classification==
*Based on the location, hypogonadism can be classified into:  
*Based on the location, hypogonadism can be classified into:  
**Primary: [[gonads]] (ovaries or testes) are the source of the disease.  
**Primary: [[gonads]] (ovaries or testes) are the primary source of the pathology.  
**Secondary (central): If the cause of the disease is the [[hypothalamus]] or [[Pituitary gland|pituitary]].  
**Secondary (central): If the cause of the disease is the [[hypothalamus]] or [[Pituitary gland|pituitary]].  
**Combined  
**Combined  

Latest revision as of 14:57, 3 October 2017

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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

Hypogonadism may be classified according to the etiological site into three subtypes namely primary, secondary or combined. Hypogonadism can also be classified according to the age into two adult and child onset disease. Also, it could be classified based on the causes into acquired or congenital.[1]

Classification

  • Based on the location, hypogonadism can be classified into:
    • Primary: gonads (ovaries or testes) are the primary source of the pathology.
    • Secondary (central): If the cause of the disease is the hypothalamus or pituitary.
    • Combined
  • Based on the age, hypogonadism can be classified into:
  • Based on the causes of the disease, hypogonadism can be classified into:

References

  1. Rey RA, Grinspon RP, Gottlieb S, Pasqualini T, Knoblovits P, Aszpis S; et al. (2013). "Male hypogonadism: an extended classification based on a developmental, endocrine physiology-based approach". Andrology. 1 (1): 3–16. doi:10.1111/j.2047-2927.2012.00008.x. PMID 23258624.

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