Document Detail


Peutz-Jeghers syndrome and family survey: a case report.
MedLine Citation:
PMID:  23638235     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Peutz-Jeghers syndrome (PJS) is a rare inherited autosomal dominant disease characterized by mucocutaneous pigmentation and multiple polyps in the gastrointestinal tract. We report on an 18-year-old Chinese male who complained with pigmentation on face and extremities for over 10 years. Colonoscopy revealed more than ten polyps from transverse colon to rectum. The family survey included 15 family members from three generations, and 6 PJSs (4 males and 2 females) were found. This case is reported because of its rarity of Peutz-Jeghers syndrome and the survey of family history.
Authors:
Yongjian Li; Qinghai Zeng; Zhiling Liao; Guiying Zhang; Rong Xiao; Haiquan Wen
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Publication Detail:
Type:  Case Reports; Journal Article     Date:  2013-04-15
Journal Detail:
Title:  International journal of clinical and experimental pathology     Volume:  6     ISSN:  1936-2625     ISO Abbreviation:  Int J Clin Exp Pathol     Publication Date:  2013  
Date Detail:
Created Date:  2013-05-02     Completed Date:  2013-11-27     Revised Date:  2013-12-02    
Medline Journal Info:
Nlm Unique ID:  101480565     Medline TA:  Int J Clin Exp Pathol     Country:  United States    
Other Details:
Languages:  eng     Pagination:  982-4     Citation Subset:  IM    
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MeSH Terms
Descriptor/Qualifier:
Adolescent
Female
Humans
Male
Pedigree*
Peutz-Jeghers Syndrome / complications,  pathology*
Comments/Corrections

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