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Familial Mediterranean fever

Gattorno, Marco.

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Familial Mediterranean fever

紀錄類型:	書目-電子資源 : Monograph/item
正題名/作者:	Familial Mediterranean fever/ edited by Marco Gattorno.
其他作者:	Gattorno, Marco.
出版者:	Cham :Springer International Publishing : : 2015.,
面頁冊數:	vii, 162 p. :ill. (some col.), digital ;24 cm.
內容註:	Preface -- 1 Genetics -- 2 Pathogenesis -- 3 Clinical Picture in Childhood -- 4 Clinical Picture in Adulthood and Unusual Clinical Features -- 5 FMF in Western Countries -- 6 Long Term Complications in FMF -- 7 Recent advances in quantitative assessment of FMF -- 8 How to Manage FMF Patients in Daily Practice -- 9 New Emerging Treatments -- Subject Index.
Contained By:	Springer eBooks
標題:	Periodic peritonitis. -
電子資源:	http://dx.doi.org/10.1007/978-3-319-14615-7
ISBN:	9783319146157 (electronic bk.)

Familial Mediterranean fever
Familial Mediterranean fever[electronic resource] /edited by Marco Gattorno. - Cham :Springer International Publishing :2015. - vii, 162 p. :ill. (some col.), digital ;24 cm. - Rare diseases of the immune system,2282-6505. - Rare diseases of the immune system..

Preface -- 1 Genetics -- 2 Pathogenesis -- 3 Clinical Picture in Childhood -- 4 Clinical Picture in Adulthood and Unusual Clinical Features -- 5 FMF in Western Countries -- 6 Long Term Complications in FMF -- 7 Recent advances in quantitative assessment of FMF -- 8 How to Manage FMF Patients in Daily Practice -- 9 New Emerging Treatments -- Subject Index.

This book, written by very well known opinion leaders in the field, covers all aspects of familial Mediterranean fever, the most common monogenic autoinflammatory disease. The opening chapters explain the genetic basis of the disease and provide insights into the pathogenesis derived from recent experimental studies. A large part of the book is then devoted to a detailed description of the typical and atypical clinical presentations, the disease course, and potential complications in both pediatric and adult patients. Guidance is provided on the measurement of disease severity and the management of patients in daily practice. The advice regarding treatment is based on the best currently available evidence and attention is also paid to important emerging treatments. The book is part of Springer's series Rare Diseases of the Immune System, which presents recently acquired knowledge on pathogenesis, diagnosis, and therapy with the aim of promoting a more holistic approach to these conditions. Monogenic autoinflammatory diseases are hereditary disorders that are caused by single-gene defects in innate immune regulatory pathways and are characterized by a clinical and biological inflammatory syndrome in which there is limited, if any, evidence of autoimmunity. Familial Mediterranean fever itself is due to a mutation in the MEFV gene, which codes for the protein pyrin; it is characterized by periodic fever and episodes of painful inflammation in the abdomen, chest, and joints. Familial Mediterranean Fever will be an invaluable source of up-to-date information for all practitioners involved in the care of patients with the disease.

ISBN: 9783319146157 (electronic bk.)

Standard No.: 10.1007/978-3-319-14615-7doiSubjects--Topical Terms:

2139677
Periodic peritonitis.

LC Class. No.: RB148

Dewey Class. No.: 616.047

Familial Mediterranean fever
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520 $a This book, written by very well known opinion leaders in the field, covers all aspects of familial Mediterranean fever, the most common monogenic autoinflammatory disease. The opening chapters explain the genetic basis of the disease and provide insights into the pathogenesis derived from recent experimental studies. A large part of the book is then devoted to a detailed description of the typical and atypical clinical presentations, the disease course, and potential complications in both pediatric and adult patients. Guidance is provided on the measurement of disease severity and the management of patients in daily practice. The advice regarding treatment is based on the best currently available evidence and attention is also paid to important emerging treatments. The book is part of Springer's series Rare Diseases of the Immune System, which presents recently acquired knowledge on pathogenesis, diagnosis, and therapy with the aim of promoting a more holistic approach to these conditions. Monogenic autoinflammatory diseases are hereditary disorders that are caused by single-gene defects in innate immune regulatory pathways and are characterized by a clinical and biological inflammatory syndrome in which there is limited, if any, evidence of autoimmunity. Familial Mediterranean fever itself is due to a mutation in the MEFV gene, which codes for the protein pyrin; it is characterized by periodic fever and episodes of painful inflammation in the abdomen, chest, and joints. Familial Mediterranean Fever will be an invaluable source of up-to-date information for all practitioners involved in the care of patients with the disease.
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