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Primary immunodeficiency diseasesdef...

Aghamohammadi, Asghar.

Primary immunodeficiency diseasesdefinition, diagnosis, and management /

Record Type:	Electronic resources : Monograph/item
Title/Author:	Primary immunodeficiency diseasesedited by Nima Rezaei, Asghar Aghamohammadi, Luigi D. Notarangelo.
Reminder of title:	definition, diagnosis, and management /
other author:	Rezaei, Nima.
Published:	Berlin, Heidelberg :Springer Berlin Heidelberg :2017.
Description:	xvii, 582 p. :ill., digital ;24 cm.
Contained By:	Springer eBooks
Subject:	Immunological deficiency syndromes.
Online resource:	http://dx.doi.org/10.1007/978-3-662-52909-6
ISBN:	9783662529096$q(electronic bk.)

Primary immunodeficiency diseasesdefinition, diagnosis, and management /
Primary immunodeficiency diseasesdefinition, diagnosis, and management /[electronic resource] :edited by Nima Rezaei, Asghar Aghamohammadi, Luigi D. Notarangelo. - 2nd ed. - Berlin, Heidelberg :Springer Berlin Heidelberg :2017. - xvii, 582 p. :ill., digital ;24 cm.

Introduction on Primary Immunodeficiency Diseases -- Combined T- and B-Cell Immunodeficiencies -- Predominantly Antibody Deficiencies -- Phagocytes Defects -- Genetic Disorders of Immune Regulation -- Defects in Intrinsic and Innate Immunity: Receptors and Signaling Components -- Autoinflammatory Disorders -- Complement Deficiencies -- Other Well-Defined Immunodeficiencies -- Syndromic Immunodeficiencies.

Primary immunodeficiency diseases (PIDs) are a group of inborn disorders of the immune system, characterized by increased susceptibility to infections, autoimmunity, and cancers. Although PIDs were previously considered rare conditions, the number of diagnosed cases is growing rapidly, and about 300 different forms of PIDs have already been recognized. Nevertheless, because of inadequate medical awareness, misdiagnosis or late diagnosis occurs in a significant number of patients, leading to avoidable morbidity and mortality. The first edition of this practical reference textbook was widely welcomed by scientists and clinicians from around the world. This new edition has been extensively revised to reflect advances in knowledge and includes various PIDs not previously covered. For each disease, information is provided on definition, etiology, clinical manifestations, diagnosis, and management. Every effort has been made to ensure that, throughout, the text is easy to read and readily comprehensible. The book will represent an ideal resource for specialists when engaging in diagnosis, clinical decision-making, and treatment planning. It will also prove invaluable for doctors in training and other physicians and nurses who wish to learn more about PIDs.

ISBN: 9783662529096$q(electronic bk.)

Standard No.: 10.1007/978-3-662-52909-6doiSubjects--Topical Terms:

277790
Immunological deficiency syndromes.

LC Class. No.: RC606 / .P747 2017

Dewey Class. No.: 616.979

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505 0 $a Introduction on Primary Immunodeficiency Diseases -- Combined T- and B-Cell Immunodeficiencies -- Predominantly Antibody Deficiencies -- Phagocytes Defects -- Genetic Disorders of Immune Regulation -- Defects in Intrinsic and Innate Immunity: Receptors and Signaling Components -- Autoinflammatory Disorders -- Complement Deficiencies -- Other Well-Defined Immunodeficiencies -- Syndromic Immunodeficiencies.
520 $a Primary immunodeficiency diseases (PIDs) are a group of inborn disorders of the immune system, characterized by increased susceptibility to infections, autoimmunity, and cancers. Although PIDs were previously considered rare conditions, the number of diagnosed cases is growing rapidly, and about 300 different forms of PIDs have already been recognized. Nevertheless, because of inadequate medical awareness, misdiagnosis or late diagnosis occurs in a significant number of patients, leading to avoidable morbidity and mortality. The first edition of this practical reference textbook was widely welcomed by scientists and clinicians from around the world. This new edition has been extensively revised to reflect advances in knowledge and includes various PIDs not previously covered. For each disease, information is provided on definition, etiology, clinical manifestations, diagnosis, and management. Every effort has been made to ensure that, throughout, the text is easy to read and readily comprehensible. The book will represent an ideal resource for specialists when engaging in diagnosis, clinical decision-making, and treatment planning. It will also prove invaluable for doctors in training and other physicians and nurses who wish to learn more about PIDs.
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