Paediatric Menetrier disease (PMD) is a protein-losing gastropathy, presenting with
generalized oedema and abdominal symptoms. PMD commonly has an acute course and …

Ménétrier's disease is a protein-losing gastropathy that is uncommon in childhood. Its
symptoms are unspecific, with abdominal pain, vomiting, and edema. Blood tests show …

We performed whole exome sequencing in individuals from a family with autosomal
dominant gastropathy resembling Ménétrier disease, a premalignant gastric disorder with …

Purpose Ménétrier disease (MD) was first described in 1888, and 50 cases have been
reported until now. We aimed to discuss the etiology, diagnostics, and management of MD in …

Diagnostic imaging of pediatric gastric masses often provides a challenge for the practicing
radiologist. Radiologists should be aware of this relatively unusual pathology, particularly in …

Pediatric Menetrier disease is a rare clinical event with unknown etiology, which has a
different course from that in adults. It is characterized by gastric hypertrophy and …

Ménétrier disease (MD) was described for the first time in 1888, and 60 cases have been
reported until now. MD is a hypertrophic gastropathy characterized by giant rugal folds …

This chapter reviews the key clinical and histological findings of the most common forms of
gastritis, focusing on diagnostically relevant questions for reactive gastropathy, peptic …

ÖZ Çocukluk çağında Menetrier hastalığı; etiyolojisi tam açıklanamamış, nadir ve seyri
erişkinlerden farklı olan klinik bir tablodur. Mide mukozasında hipertrofi ve buradan protein …

Ménétrier disease is a rare condition characterized clinically by edema caused by
hypoalbuminemia and endoscopically by hypertrophy of the gastric mucosal folds. Contrary …