合計: 3 |
|
PMID (PMCID) | ||
---|---|---|
19998717 |
MALE | |
A Japanese case of familial Mediterranean fever with a MEFV gene mutation. | ||
Kawabata H, Murakami M, Nishikomori R, Saito M, Takaoka Y, Nanao K, Maezawa M. Hokkaido Igaku Zasshi. 2009;84(6):419-22. |
||
A 17-year-old Japanese male with a three-year history of recurrent episodic chest pain and fever, each lasting for one to three days, was diagnosed with familial Mediterranean fever (FMF) because of the following: 1) short attacks of chest pain and fever recurring at varying intervals; 2) no symptoms with a sense of well-being between attacks; and 3) identification of the Mediterranean fever gene (MEFV) mutation demonstrating M6941. | ||
19998717 |
MALE | |
A Japanese case of familial Mediterranean fever with a MEFV gene mutation. | ||
Kawabata H, Murakami M, Nishikomori R, Saito M, Takaoka Y, Nanao K, Maezawa M. Hokkaido Igaku Zasshi. 2009;84(6):419-22. |
||
A 17-year-old Japanese male with a three-year history of recurrent episodic chest pain and fever, each lasting for one to three days, was diagnosed with familial Mediterranean fever (FMF) because of the following: 1) short attacks of chest pain and fever recurring at varying intervals; 2) no symptoms with a sense of well-being between attacks; and 3) identification of the Mediterranean fever gene (MEFV) mutation demonstrating M6941. | ||
15015067 |
FEMALE | Child |
Variable expression of vasculitis in siblings with familial Mediterranean fever. | ||
Lange-Sperandio B, Mohring K, Gutzler F, Mehls O. Pediatr Nephrol. 2004;19(5):539-43. |
||
Familial Mediterranean fever (FMF) is an autosomal recessive disorder characterized by recurrent and self-limited attacks of serosal inflammation with abdominal pain, chest pain, and arthritis usually accompanied by fever. |