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Clinical Cases in Primary Immunodeficiency Diseases: A Problem-Solving Approach

ISBN-13: 9783642444234 / Angielski / Miękka / 2015 / 380 str.

Asghar Aghamohammadi; Nima Rezaei
Clinical Cases in Primary Immunodeficiency Diseases: A Problem-Solving Approach Aghamohammadi, Asghar 9783642444234 Springer - książkaWidoczna okładka, to zdjęcie poglądowe, a rzeczywista szata graficzna może różnić się od prezentowanej.

Clinical Cases in Primary Immunodeficiency Diseases: A Problem-Solving Approach

ISBN-13: 9783642444234 / Angielski / Miękka / 2015 / 380 str.

Asghar Aghamohammadi; Nima Rezaei
cena 442,79
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Primary immunodeficiency diseases (PIDs) are a heterogeneous group of inherited disorders characterized by different defects in the development and function of the immune system. This book aims to increase the clinical awareness and knowledge of practicing clinicians regarding the diagnosis and management of PIDs. In order to achieve this goal, about 90 cases drawn from real life are presented, along with approximately 300 related questions. The selected case reports are the result of the invaluable cooperation of more than 40 scientists in the field of immunodeficiency. They focus both on the presenting features of patients with PIDs and on the required further investigation and management. Each of the numbered cases is followed by the questions, their answers, and additional discussion. Each question focuses on a particular aspect of the PID under consideration, and the topics covered include clinical diagnosis, laboratory findings, molecular mechanisms, and therapy.

Kategorie:
Nauka, Medycyna
Kategorie BISAC:
Medical > Immunology
Medical > Choroby zakaźne
Medical > Pediatrics
Wydawca:
Springer
Język:
Angielski
ISBN-13:
9783642444234
Rok wydania:
2015
Wydanie:
2012
Ilość stron:
380
Waga:
0.61 kg
Wymiary:
23.5 x 15.5
Oprawa:
Miękka
Wolumenów:
01
Dodatkowe informacje:
Wydanie ilustrowane

From the reviews:

"This book reviews some of the most common and important primary immunodeficiency syndromes through a series of selected cases that highlight the presenting clinical characteristics, diagnostic evaluation, including the molecular basis of the disorders, and basic treatment. ... This would be a good resource for general practitioners, pediatricians, infectious disease specialists, or hematologists who may encounter these patients. ... This book is a resource for nonimmunologists to help them recognize the clinical presentation of the primary immunodeficiency diseases." (Kari Neemann, Doody's Book Reviews, August, 2013)

Recurrent infections.- Combined T- and B-cell immunodeficiencies.- Primary Antibody Deficiencies.- Disorders of Phagocytic Cells.- Immune dysregulation diseases.- Defects in Innate immunity: Receptors and Signaling Components.- Autoinflammatory disorders.- Complement deficiencies.- Other well-defined immunodeficiency syndromes.

 

Primary immunodeficiency diseases (PIDs) are a heterogeneous group of inherited disorders characterized by different defects in the development and function of the immune system. These defects render patients susceptible to a variety of infectious diseases. Knowledge of normal immunity and specific warning signs and symptoms can help physicians to identify those children with underlying PIDs.

This book aims to increase the clinical awareness and knowledge of practicing clinicians regarding the diagnosis and management of PIDs. In order to achieve this goal, about 90 cases drawn from real life are presented, along with approximately 300 related questions. The selected case reports are the result of the invaluable cooperation of more than 40 scientists in the field of immunodeficiency. They focus both on the presenting features of patients with PIDs and on the required further investigation and management. Although the case scenarios relate to real histories, some modifications have been made for educational purposes. Each of the numbered cases is followed by the questions, their answers, and additional discussion. Each question focuses on a particular aspect of the PID under consideration, and the topics covered include clinical diagnosis, laboratory findings, molecular mechanisms, and therapy.

This practical, case-oriented book will be an invaluable source of guidance on the diagnosis and treatment of patients with PIDs and will be relevant for those working in a variety of specialties and subspecialties.



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