Hereditary pancreatitis: Difference between revisions

Jump to navigation Jump to search
No edit summary
(Blanked the page)
Line 1: Line 1:
__NOTOC__
{{SI}}
'''For patient information click [[{{PAGENAME}} (patient information)|here]]'''


'''For full discussion on Pancreatitis click [[Pancreatitis|here]].'''
{{CMG}}
==Overview==
'''Hereditary Pancreatitis''' is a genetic disease affecting enzyme production in the pancreas.
==Pathophysiology==
In the pancreas, a genetic mutation causes the enzyme [[trypsinogen]] to be made in a way which renders it resistant to inactivation through [[autolysis]]. Normally this autolysis mechanism prevents trypsinogen from being activated within the pancreas. However, when the abnormal trypsinogen is activated, it causes a chain reaction where all the trypsinogen in the pancreas is activated, effectively digesting the pancreas from the inside.
==Epidemiology and Demographics==
===Prevalence===
Most estimates place the number of individuals with hereditary pancreatitis in the United States at 1000.
==Diagnosis==
===History and Symptoms===
Symptoms are generally the same as [[acute pancreatitis]], including
* Severe [[abdominal pain]]
* [[Vomiting]]
* [[Diarrhea]]
==Treatment==
===Medical Therapy===
There is no treatment for the disease, although complications such as malnutrition can be treated with supplimentary pancreatic enzymes.
==References==
{{reflist|2}}
{{Gastroenterology}}
[[Category:Gastroenterology]]
[[Category:Genetic disorders]]
[[Category:Disease]]
{{WikiDoc Help Menu}}
{{WikiDoc Sources}}
'''Bold text'''

Revision as of 14:28, 26 October 2017