Peutz-Jeghers syndrome differential diagnosis: Difference between revisions

	Peutz-Jeghers syndrome Microchapters
Home
Patient Information
Overview
Historical Perspective
Classification
Pathophysiology
Causes
Differentiating Peutz-Jeghers syndrome from other Diseases
Epidemiology and Demographics
Risk Factors
Screening
Natural history, Complications and Prognosis
Diagnosis
Diagnostic Study of Choice
History and Symptoms
Physical Examination
Laboratory Findings
Chest X Ray
CT
MRI
Ultrasound
Other Imaging Findings
Other Diagnostic Studies
Treatment
Medical Therapy
Surgery
Primary Prevention
Secondary Prevention
Cost-Effectiveness of Therapy
Future or Investigational Therapies
Case Studies
Case #1
Peutz-Jeghers syndrome differential diagnosis On the Web
Most recent articles
Most cited articles
Review articles
CME Programs
Powerpoint slides
Images
American Roentgen Ray Society Images of Peutz-Jeghers syndrome differential diagnosis All Images X-rays Echo & Ultrasound CT Images MRI
Ongoing Trials at Clinical Trials.gov
US National Guidelines Clearinghouse
NICE Guidance
FDA on Peutz-Jeghers syndrome differential diagnosis
CDC on Peutz-Jeghers syndrome differential diagnosis
Peutz-Jeghers syndrome differential diagnosis in the news
Blogs on Peutz-Jeghers syndrome differential diagnosis
Directions to Hospitals Treating Peutz-Jeghers syndrome
Risk calculators and risk factors for Peutz-Jeghers syndrome differential diagnosis

Revision as of 15:22, 12 September 2012

Please help WikiDoc by adding more content here. It's easy! Click here to learn about editing.

@@ Line 1: / Line 1: @@
+__NOTOC__
 {{Peutz-Jeghers syndrome}}
-{{CMG}}
+Please help WikiDoc by adding more content here.  It's easy!  Click  [[Help:How_to_Edit_a_Page|here]]  to learn about editing.
-==Overview==
-'''Peutz-Jeghers''', also known as '''Hereditary Intestinal Polyposis Syndrome''', is an [[autosomal dominant]] [[genetic disease]] characterized by the development of benign hamartomatous polyps in the gastrointestinal tract.
 == References ==
@@ Line 18: / Line 16: @@
 [[Category:Oncology]]
 [[Category:Syndromes]]
+[[Category:Needs content]]
 [[de:Peutz-Jeghers-Syndrom]]

v t e Phakomatosis (Q85, 759.5–759.6)
Angiomatosis	Sturge–Weber syndrome Von Hippel–Lindau disease
Hamartoma	Tuberous sclerosis Hypothalamic hamartoma (Pallister–Hall syndrome) Multiple hamartoma syndrome Proteus syndrome Cowden syndrome Bannayan–Riley–Ruvalcaba syndrome Lhermitte–Duclos disease
Neurofibromatosis	Type I Type II
Other	Abdallat–Davis–Farrage syndrome Ataxia telangiectasia Incontinentia pigmenti Peutz–Jeghers syndrome Encephalocraniocutaneous lipomatosis