Peutz–Jeghers syndrome

Background: Peutz-Jeghers syndrome (PJS) is an autosomal dominant condition presenting with mucocutaneous pigmentation. We report a rare condition of PJS in an 11-year-old female. Case Presentation: An 11-year-old girl, previously healthy and developmental^ normal, presented to the emergency departm...

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Veröffentlicht in:	European Journal of Medical Case Reports 2020, Vol.4 (2), p.70-74
Hauptverfasser:	Shahzadi, Nagina, Hashmat, Nadeem, Satti, Naureen Kanwal, Tabassum, Lubna
Format:	Artikel
Sprache:	eng
Schlagworte:	Case reports Gastrointestinal diseases Genetic disorders Medical diagnosis Mutation Pediatrics Polyps
Online-Zugang:	Volltext
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