<p><strong>Background: </strong>Peutz-Jeghers syndrome is a rare genetic disorder presenting in young age with mucocutaneous pigmentation and hamartomatous polyposis. <strong>Method:</strong> We report a case of Peutz-Jeghers syndrome in a 16 year old boy presenting with acute intestinal obstruction. <strong>Results:</strong> Imaging studies revealed intussusception. He had mucocutaneous pigmentation and multiple hamartomatous polyps which were diagnosed histologically. The unusual presentation of the case and its successful management has prompted us to report the case with literature review.</p
The aim of this paper is to present a rare case of Peutz–Jeghers syndrome and review the literature....
Peutz-Jeghers syndrome (PJS) is characterized by multiple hamartomatous polyps in the gastrointestin...
Peutz-Jeghers syndrome is a rare autosomal dominant polyposis characterized by mucocutaneous pigment...
Peutz-jeghers syndrome is rare condition with autosomal dominant inheritance. It is due to the mutat...
The authors describe the case of a 7 year old boy who presented an intestinal intussusception due to...
Peutz-Jeghers syndrome is a rare inherited condition characterized by hamartomatous gastrointestinal...
Peutz-Jeghers syndrome is characterized mainly by the presence of hamartomatous polyposis of gastroi...
Peutz-Jeghers syndrome is a rare autosomal dominant disorder of hamartomatous polyposis of the gastr...
Peutz Jeghers Syndrome (PJS), which was first described in 1921 by Peutz, followed by Jeghers etal i...
An 18-year-old male patient presenting with mucocutaneous lesions of the face, chronic recurring abd...
AbstractPJS is an autosomal dominant genetic disease associated with melanin pigment spots on the or...
Peutz-Jeghers syndrome (PJS) is a rare autosomal dominant disorder characterized by typical pigmente...
Introduction: Peutz-Jeghers syndrome (PJS) is a rare familial disorder characterised by mucocutaneou...
Peutz-Jeghers syndrome is an autosomal dominant inherited disorder characterized by hamartomatous po...
Peutz-Jeghers syndrome (PSJ) is a relatively rare but well-recognized condition, with a prevalence o...
The aim of this paper is to present a rare case of Peutz–Jeghers syndrome and review the literature....
Peutz-Jeghers syndrome (PJS) is characterized by multiple hamartomatous polyps in the gastrointestin...
Peutz-Jeghers syndrome is a rare autosomal dominant polyposis characterized by mucocutaneous pigment...
Peutz-jeghers syndrome is rare condition with autosomal dominant inheritance. It is due to the mutat...
The authors describe the case of a 7 year old boy who presented an intestinal intussusception due to...
Peutz-Jeghers syndrome is a rare inherited condition characterized by hamartomatous gastrointestinal...
Peutz-Jeghers syndrome is characterized mainly by the presence of hamartomatous polyposis of gastroi...
Peutz-Jeghers syndrome is a rare autosomal dominant disorder of hamartomatous polyposis of the gastr...
Peutz Jeghers Syndrome (PJS), which was first described in 1921 by Peutz, followed by Jeghers etal i...
An 18-year-old male patient presenting with mucocutaneous lesions of the face, chronic recurring abd...
AbstractPJS is an autosomal dominant genetic disease associated with melanin pigment spots on the or...
Peutz-Jeghers syndrome (PJS) is a rare autosomal dominant disorder characterized by typical pigmente...
Introduction: Peutz-Jeghers syndrome (PJS) is a rare familial disorder characterised by mucocutaneou...
Peutz-Jeghers syndrome is an autosomal dominant inherited disorder characterized by hamartomatous po...
Peutz-Jeghers syndrome (PSJ) is a relatively rare but well-recognized condition, with a prevalence o...
The aim of this paper is to present a rare case of Peutz–Jeghers syndrome and review the literature....
Peutz-Jeghers syndrome (PJS) is characterized by multiple hamartomatous polyps in the gastrointestin...
Peutz-Jeghers syndrome is a rare autosomal dominant polyposis characterized by mucocutaneous pigment...