Familial mediterranean fever and other autoinflammatory disorders

Hatem El-Shanti, Hasan Abdel Majeed

Research output: Chapter in Book/Report/Conference proceedingChapter

Abstract

Autoinflammatory diseases are a group of disorders characterized by seemingly unprovoked inflammation in the absence of high-titer autoantibodies or antigen-specific T-cells (Stojanov and Kastner 2005). The autoinflammatory diseases include the hereditary periodic fever syndromes and are thought to be due to disturbances in the regulation of the innate immunity (Kastner 2005). Familial Mediterranean Fever (FMF) is the archetypal hereditary periodic fever syndrome and autoinflammatory disease. Other disorders include tumor necrosis factor receptor-associated periodic syndrome (TRAPS); hyperimmunoglobulinemia D with periodic fever syndrome (Hyper-IgD); pyogenic arthritis, pyoderma gangrenosum, and acne (PAPA) syndrome; the cryopyrinopathies: familial cold autoinflammatory syndrome (FCAS), Muckle-Wells syndrome (MWS), and neonatal-onset multisystem inflammatory disease (NOMID, also called chronic infantile neurologic cutaneous and articular syndrome, or CINCA syndrome); and chronic recurrent multifocal osteomyelitis (McGonagle and McDermott 2006; Milhavet et al. 2008).

Original languageEnglish
Title of host publicationGenetic Disorders Among Arab Populations
PublisherSpringer-Verlag Berlin Heidelberg
Pages111-143
Number of pages33
ISBN (Print)9783642050800, 9783642050794
DOIs
Publication statusPublished - 2010

Fingerprint

Cryopyrin-Associated Periodic Syndromes
Familial Mediterranean Fever
Hereditary Autoinflammatory Diseases
Mevalonate Kinase Deficiency
Immunoglobulin D
T-cells
Tumor Necrosis Factor Receptors
Autoantibodies
Antigens
Innate Immunity
Fever
Inflammation
T-Lymphocytes

ASJC Scopus subject areas

  • Medicine(all)
  • Biochemistry, Genetics and Molecular Biology(all)

Cite this

El-Shanti, H., & Majeed, H. A. (2010). Familial mediterranean fever and other autoinflammatory disorders. In Genetic Disorders Among Arab Populations (pp. 111-143). Springer-Verlag Berlin Heidelberg. https://doi.org/10.1007/978-3-642-05080-0_5

Familial mediterranean fever and other autoinflammatory disorders. / El-Shanti, Hatem; Majeed, Hasan Abdel.

Genetic Disorders Among Arab Populations. Springer-Verlag Berlin Heidelberg, 2010. p. 111-143.

Research output: Chapter in Book/Report/Conference proceedingChapter

El-Shanti, H & Majeed, HA 2010, Familial mediterranean fever and other autoinflammatory disorders. in Genetic Disorders Among Arab Populations. Springer-Verlag Berlin Heidelberg, pp. 111-143. https://doi.org/10.1007/978-3-642-05080-0_5
El-Shanti H, Majeed HA. Familial mediterranean fever and other autoinflammatory disorders. In Genetic Disorders Among Arab Populations. Springer-Verlag Berlin Heidelberg. 2010. p. 111-143 https://doi.org/10.1007/978-3-642-05080-0_5
El-Shanti, Hatem ; Majeed, Hasan Abdel. / Familial mediterranean fever and other autoinflammatory disorders. Genetic Disorders Among Arab Populations. Springer-Verlag Berlin Heidelberg, 2010. pp. 111-143
@inbook{3742e3bbc9a14249a716e6b16e881cc9,
title = "Familial mediterranean fever and other autoinflammatory disorders",
abstract = "Autoinflammatory diseases are a group of disorders characterized by seemingly unprovoked inflammation in the absence of high-titer autoantibodies or antigen-specific T-cells (Stojanov and Kastner 2005). The autoinflammatory diseases include the hereditary periodic fever syndromes and are thought to be due to disturbances in the regulation of the innate immunity (Kastner 2005). Familial Mediterranean Fever (FMF) is the archetypal hereditary periodic fever syndrome and autoinflammatory disease. Other disorders include tumor necrosis factor receptor-associated periodic syndrome (TRAPS); hyperimmunoglobulinemia D with periodic fever syndrome (Hyper-IgD); pyogenic arthritis, pyoderma gangrenosum, and acne (PAPA) syndrome; the cryopyrinopathies: familial cold autoinflammatory syndrome (FCAS), Muckle-Wells syndrome (MWS), and neonatal-onset multisystem inflammatory disease (NOMID, also called chronic infantile neurologic cutaneous and articular syndrome, or CINCA syndrome); and chronic recurrent multifocal osteomyelitis (McGonagle and McDermott 2006; Milhavet et al. 2008).",
author = "Hatem El-Shanti and Majeed, {Hasan Abdel}",
year = "2010",
doi = "10.1007/978-3-642-05080-0_5",
language = "English",
isbn = "9783642050800",
pages = "111--143",
booktitle = "Genetic Disorders Among Arab Populations",
publisher = "Springer-Verlag Berlin Heidelberg",

}

TY - CHAP

T1 - Familial mediterranean fever and other autoinflammatory disorders

AU - El-Shanti, Hatem

AU - Majeed, Hasan Abdel

PY - 2010

Y1 - 2010

N2 - Autoinflammatory diseases are a group of disorders characterized by seemingly unprovoked inflammation in the absence of high-titer autoantibodies or antigen-specific T-cells (Stojanov and Kastner 2005). The autoinflammatory diseases include the hereditary periodic fever syndromes and are thought to be due to disturbances in the regulation of the innate immunity (Kastner 2005). Familial Mediterranean Fever (FMF) is the archetypal hereditary periodic fever syndrome and autoinflammatory disease. Other disorders include tumor necrosis factor receptor-associated periodic syndrome (TRAPS); hyperimmunoglobulinemia D with periodic fever syndrome (Hyper-IgD); pyogenic arthritis, pyoderma gangrenosum, and acne (PAPA) syndrome; the cryopyrinopathies: familial cold autoinflammatory syndrome (FCAS), Muckle-Wells syndrome (MWS), and neonatal-onset multisystem inflammatory disease (NOMID, also called chronic infantile neurologic cutaneous and articular syndrome, or CINCA syndrome); and chronic recurrent multifocal osteomyelitis (McGonagle and McDermott 2006; Milhavet et al. 2008).

AB - Autoinflammatory diseases are a group of disorders characterized by seemingly unprovoked inflammation in the absence of high-titer autoantibodies or antigen-specific T-cells (Stojanov and Kastner 2005). The autoinflammatory diseases include the hereditary periodic fever syndromes and are thought to be due to disturbances in the regulation of the innate immunity (Kastner 2005). Familial Mediterranean Fever (FMF) is the archetypal hereditary periodic fever syndrome and autoinflammatory disease. Other disorders include tumor necrosis factor receptor-associated periodic syndrome (TRAPS); hyperimmunoglobulinemia D with periodic fever syndrome (Hyper-IgD); pyogenic arthritis, pyoderma gangrenosum, and acne (PAPA) syndrome; the cryopyrinopathies: familial cold autoinflammatory syndrome (FCAS), Muckle-Wells syndrome (MWS), and neonatal-onset multisystem inflammatory disease (NOMID, also called chronic infantile neurologic cutaneous and articular syndrome, or CINCA syndrome); and chronic recurrent multifocal osteomyelitis (McGonagle and McDermott 2006; Milhavet et al. 2008).

UR - http://www.scopus.com/inward/record.url?scp=84920429455&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=84920429455&partnerID=8YFLogxK

U2 - 10.1007/978-3-642-05080-0_5

DO - 10.1007/978-3-642-05080-0_5

M3 - Chapter

AN - SCOPUS:84920429455

SN - 9783642050800

SN - 9783642050794

SP - 111

EP - 143

BT - Genetic Disorders Among Arab Populations

PB - Springer-Verlag Berlin Heidelberg

ER -