منابع مشابه
Hereditary periodic fever syndromes.
The hereditary periodic fevers are a group of Mendelian disorders characterized by seemingly unprovoked fever and localized inflammation. Recent data indicate that these illnesses represent inborn errors in the regulation of innate immunity. Pyrin, the protein mutated in familial Mediterranean fever, defines an N-terminal domain found in a large family of proteins involved in inflammation and a...
متن کاملHereditary periodic fever syndromes
osting by E Abstract Hereditary periodic fever syndromes, comprise a group of hereditary disorders with similar clinical features of recurrent short episodes of fever associated with inflammatory manifestations. These are usually self-limited in nature and occur in the absence of infection or autoimmune reaction. Between attacks, patients feel well and regain their normal daily functions until ...
متن کاملPeriodic Fever Panel
The Periodic Fever Syndrome Panel provides a high quality read-out of all clinically relevant genes associated with hereditary fever. Our OS-SeqTM technology provides high coverage clinical grade sequencing and enables reliable diagnostics for patients with significantly lower costs and faster turnaround time (basic service TAT 21 days and Express service TAT 7-10 days). The Periodic Fever Synd...
متن کاملNeither hereditary periodic fever nor periodic fever, aphthae, pharingitis, adenitis: Undifferentiated periodic fever in a tertiary pediatric center
AIM To describe the frequency and clinical characteristics of patients with undifferentiated periodic fever (UPF) and to investigate whether a clinical classification of UPF based on the PRINTO-Eurofever score can help predicting the response to treatment and the outcome at follow-up. METHODS Clinical and therapeutic information of patients with recurrent fever who presented at a single pedia...
متن کاملPeriodic Fever: a Case Report
In this report, we describe the case of a twenty-year-old woman, with recurrent fever, accompanied by shaking chills and followed by profuse sweating, bilateral diffuse arthralgia and evidence of focal myositis, associated with elevation of inflammatory markers, pancytopenia, hypocholesterolemia, and hepatosplenomegaly, unresponsive to antibiotic therapy. Subsequently to the exclusion of infect...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
ژورنال
عنوان ژورنال: BMJ
سال: 1974
ISSN: 0959-8138,1468-5833
DOI: 10.1136/bmj.4.5938.232-b