Periodic fever syndromes

被引:26
作者
Scholl, PR [1 ]
机构
[1] Northwestern Univ, Sch Med, Childrens Mem Hosp, Dept Pediat,Div Immunol Rheumatol, Chicago, IL USA
关键词
D O I
10.1097/00008480-200012000-00009
中图分类号
R72 [儿科学];
学科分类号
100202 [儿科学];
摘要
The term periodic fever syndrome has been used in a restricted sense to denote two diseases in which episodic fevers occur with a regular periodicity: cyclic neutropenia and the periodic fever, aphthous stomatitis, pharyngitis, and adenopathy (PFAPA) syndrome, Other authors have used the term in a more general sense to encompass a larger group of disorders characterized by recurrent episodes of fever that do not necessarily follow a strictly periodic pattern. These include familiar Mediterranean fever, the autosomal dominant familial fevers (also known as Hibernian fever), and the hyper-immunoglobulin D syndrome. This article follows the latter usage, and reviews recent advances in our understanding of the genetics and molecular pathology of this group of diseases, as well as their clinical characterization and treatment. (C) 2000 Lippincott Williams & Wilkins, Inc.
引用
收藏
页码:563 / 566
页数:4
相关论文
共 33 条
[1]
Mutation and haplotype studies of familial Mediterranean fever reveal new ancestral relationships and evidence for a high carrier frequency with reduced penetrance in the Ashkenazi Jewish population [J].
Aksentijevich, I ;
Torosyan, Y ;
Samuels, J ;
Centola, M ;
Pras, E ;
Chae, JJ ;
Oddoux, C ;
Wood, G ;
Azzaro, MP ;
Palumbo, G ;
Giustolisi, R ;
Pras, M ;
Ostrer, H ;
Kastner, DL .
AMERICAN JOURNAL OF HUMAN GENETICS, 1999, 64 (04) :949-962
[2]
Aksentijevich I, 1997, CELL, V90, P797
[3]
Bernot A, 1997, NAT GENET, V17, P25
[4]
Familial Mediterranean fever: Clinical and genetic characterization in a mixed pediatric population of Jewish and Arab patients [J].
Brik, R ;
Shinawi, M ;
Kepten, I ;
Berant, M ;
Gershoni-Baruch, R .
PEDIATRICS, 1999, 103 (05)
[5]
MEFV-gene analysis in Armenian patients with familial Mediterranean fever:: Diagnostic value and unfavorable renal prognosis of the M694V homozygous genotype -: Genetic and therapeutic implications [J].
Cazeneuve, C ;
Sarkisian, T ;
Pêcheux, C ;
Dervichian, M ;
Nédelec, B ;
Reinert, P ;
Ayvazyan, A ;
Kouyoumdjian, JC ;
Ajrapetyan, H ;
Delpech, M ;
Goossens, M ;
Dodé, C ;
Grateau, G ;
Amselem, S .
AMERICAN JOURNAL OF HUMAN GENETICS, 1999, 65 (01) :88-97
[6]
The gene for familial Mediterranean fever, MEFV, is expressed in early leukocyte development and is regulated in response to inflammatory mediators [J].
Centola, M ;
Wood, G ;
Frucht, DM ;
Galon, J ;
Aringer, M ;
Farrell, C ;
Kingma, DW ;
Horwitz, ME ;
Mansfield, E ;
Holland, SM ;
O'Shea, JJ ;
Rosenberg, HF ;
Malech, HL ;
Kastner, DL .
BLOOD, 2000, 95 (10) :3223-3231
[7]
Direskeneli H, 1999, J RHEUMATOL, V26, P1983
[8]
HYPERIMMUNOGLOBULINEMIA-D AND PERIODIC FEVER SYNDROME - THE CLINICAL SPECTRUM IN A SERIES OF 50 PATIENTS [J].
DRENTH, JPH ;
HAAGSMA, CJ ;
VANDERMEER, JWM ;
WEEMAES, CMR ;
BIJLSMA, JWJ ;
DEGRAEFFMEEDER, ER ;
ALCALAY, M ;
CHAPELONABRIC, C ;
KAHN, MF ;
PRIEUR, AM ;
SIBILIA, J ;
POWELL, RJ ;
TOPALOGLU, R ;
SAATCI, U ;
SCOLOZZI, R ;
LAZZARIN, P ;
MONCIOTTI, CM ;
DEMONTY, J ;
JILEK, D ;
MIYAGAWA, S ;
ESPANOL, T .
MEDICINE, 1994, 73 (03) :133-144
[9]
Mutations in the gene encoding mevalonate kinase cause hyper-IgD and periodic fever syndrome [J].
Drenth, JPH ;
Cuisset, L ;
Grateau, G ;
Vasseur, C ;
van de Velde-Visser, SD ;
de Jong, JGN ;
Beckmann, JS ;
van der Meer, JWM ;
Delpech, M .
NATURE GENETICS, 1999, 22 (02) :178-181
[10]
CYTOKINE ACTIVATION DURING ATTACKS OF THE HYPERIMMUNOGLOBULINEMIA-D AND PERIODIC FEVER SYNDROME [J].
DRENTH, JPH ;
VANDEUREN, M ;
VANDERVENJONGEKRIJG, J ;
SCHALKWIJK, CG ;
VANDERMEER, JWM .
BLOOD, 1995, 85 (12) :3586-3593