An unusual presentation of familial Mediterranean fever with co-existing
polyarteritis nodosa and acute post-streptococcal glomerulonephritis
- yesim ozdemir atikel
, - Betul Emine Derinkuyu,
- Sevcan Bakkaloğlu
Betul Emine Derinkuyu
Gazi University Faculty of Medicine
Author ProfileAbstract
The homozygous M694V mutation in the MEFV gene may cause an augmented
response to the streptococcal infection that plays a role in the
development of APSGN and PAN. Both clinical manifestations may occur
simultaneously after streptococcal infection in a child who is
previously healthy but carries a MEFV mutation.11 Nov 2021Submitted to Clinical Case Reports 12 Nov 2021Submission Checks Completed
12 Nov 2021Assigned to Editor
23 Nov 2021Reviewer(s) Assigned
07 Dec 2021Review(s) Completed, Editorial Evaluation Pending
25 Dec 2021Editorial Decision: Revise Minor
05 Mar 20221st Revision Received
07 Mar 2022Submission Checks Completed
07 Mar 2022Assigned to Editor
07 Mar 2022Review(s) Completed, Editorial Evaluation Pending
22 May 2022Editorial Decision: Accept
