1.
Magy Seb
; 72(3): 107-111, 2019 Sep.
Article
in Hungarian
| MEDLINE
| ID: mdl-31544480
ABSTRACT
Introduction: Gardner's syndrome is a clinical subgroup of Familial Adenomatosus Polyposis, arare, autosomal disease. It is characterized by gastrointestinal polyps and extra-intestinal manifestations including multiple osteomas, skin and tissue tumours. The authors describe a case of a male patient, and discuss the diagnosis, treatment and follow-up of patients with Gardner's syndrome. We conclude that the knowledge of rare syndromes is very important for the correct treatment.
Subject(s)
Gardner Syndrome/diagnosis , Gardner Syndrome/therapy , Adenomatous Polyposis Coli/pathology , Adult , Fibromatosis, Aggressive/pathology , Gardner Syndrome/pathology , Humans , Male , Rare Diseases
2.
Magy Seb
; 61(4): 215-6, 2008 Aug.
Article
in Hungarian
| MEDLINE
| ID: mdl-18799404