Book Review: Primary Immunodeficiency Diseases

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چکیده

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منابع مشابه

A Review of Primary Immunodeficiency Diseases with Skin Manifestations

Introduction: Primary immunodeficiencies (PID) are rare heterogeneous disorders with defects in which one or more components of the immune system are malfunctioning. Clinical presentations of the patients according to type of immunodeficiency are variable. The majority of these patients are susceptible to infections depending on the type of disorder. In these patients, one of the most important...

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Prevalence of Primary Immunodeficiency Diseases in Kerman, Southeast of Iran

Objective: Primary immunodeficiency diseases (PID) are rare and heterogeneous congenital diseases leading to increased unusual susceptibility to developing infections and causingsome malignancies and autoimmune diseases. This study was conducted to evaluate the epidemiological characteristics of primary these diseases in patients attending the clinic of immunodeficiency diseases in Kerman.Subje...

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Primary Immunodeficiency Diseases

The abstracts that are presented following these individual papers are difficult to evaluate because they do not contain detailed data. However, some interesting results are presented which can be better evaluated when published in full. Examples include a categorization of congenital malformations among births in Puerto Rico, a piece of epidemiologic data not previously available, a presentati...

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Bone and joint manifestations of primary immunodeficiency patients: review article

Primary Immune Deficiencies are a group of heterogeneous disorders that involve the innate or acquired immune system, or a combination of them. The underlying disorder may be related to decreased levels or function, or a complete lack of one or more components of the immune system in general. These diseases can occur with a prevalence of about 1 in 10000 live births. According to the fourth upd...

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ژورنال

عنوان ژورنال: Journal of the Royal Society of Medicine

سال: 1985

ISSN: 0141-0768,1758-1095

DOI: 10.1177/014107688507800246