Peutz-Jeghers syndrome ultrasound: Difference between revisions

	Peutz-Jeghers syndrome Microchapters
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Revision as of 15:30, 12 September 2012

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-==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 ==
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+[[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