Hypopituitarism classification: Difference between revisions

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==Classification==
==Classification==
Hypopituitarism can be classified based on the following different ways of classification:  
Hypopituitarism can be classified based on the following different ways of classification:<ref name="Lambertsde Herder1998">{{cite journal|last1=Lamberts|first1=SWJ|last2=de Herder|first2=WW|last3=van der Lely|first3=AJ|title=Pituitary insufficiency|journal=The Lancet|volume=352|issue=9122|year=1998|pages=127–134|issn=01406736|doi=10.1016/S0140-6736(98)85043-5}}</ref>
*Etiology:  
*Etiology:  
**Primary hypopituitarism  
**Primary hypopituitarism  
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***[[Anterior]]   
***[[Anterior]]   
***[[Posterior]]   
***[[Posterior]]   
**[[Panhypopituitarism]]  
**[[Panhypopituitarism]]


==References==
==References==

Revision as of 18:33, 20 September 2017

Hypopituitarism Microchapters

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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

Hypopituitarism can be classified according to the site of the affected part of the pituitary gland either anterior or posterior. It can be also classified according to the etiology into primary or secondary. Based on the gland involvement, hypopituitarism can be classified into partial and panhypopituitarism.

Classification

Hypopituitarism can be classified based on the following different ways of classification:[1]

References

  1. Lamberts, SWJ; de Herder, WW; van der Lely, AJ (1998). "Pituitary insufficiency". The Lancet. 352 (9122): 127–134. doi:10.1016/S0140-6736(98)85043-5. ISSN 0140-6736.

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