Delayed diagnosis of Peutz–Jeghers syndrome due to pathological information loss or mistake in family/personal history

Abstract Objective To report Peutz–Jeghers syndrome (PJS) cases with non-definitive clues in the family or personal history and finally diagnosed through pathological examination and STK11 gene mutation test. Clinical presentation and intervention PJS was suspected in 3 families with tortuous medica...

תיאור מלא

מידע ביבליוגרפי

Principais autores:	Yu-Liang Jiang, Xiao-Dong Xu, Bai-Rong Li, En-Da Yu, Zi-Ye Zhao, Hong Liu
פורמט:	Artigo
שפה:	Inglês
יצא לאור:	BMC 2021-06-01
סדרה:	Orphanet Journal of Rare Diseases
נושאים:	Peutz–Jeghers syndrome STK11 gene Hamartoma Polyposis Enteroscopy
גישה מקוונת:	https://doi.org/10.1186/s13023-021-01900-7
תגים:	הוספת תג אין תגיות, היה/י הראשונ/ה לתייג את הרשומה!