Abstract
The article presents a clinical case of a 33-year-old Armenian man, who suffered from two rare diseases: Familial Mediterranean fever and celiac. The diagnosis of Familial Mediterranean fever: abdominal-feverish form, is confirmed by genetic markers. The morphological study of duodenal mucosa's specimens confirms the celiac.
MeSH terms
-
Adult
-
Celiac Disease / complications*
-
Celiac Disease / diagnosis
-
Celiac Disease / pathology
-
Cytoskeletal Proteins / genetics
-
Diagnosis, Differential
-
Duodenum / pathology
-
Familial Mediterranean Fever / complications*
-
Familial Mediterranean Fever / diagnosis
-
Familial Mediterranean Fever / genetics
-
Genetic Markers
-
Humans
-
Intestinal Mucosa / pathology
-
Male
-
Pyrin
Substances
-
Cytoskeletal Proteins
-
Genetic Markers
-
MEFV protein, human
-
Pyrin