Familial Mediterranean Fever in Children

Familial Mediterranean Fever in Children
Author: Abraham Gedalia
Publsiher: Anonim
Total Pages: 17
Release: 1992
ISBN 10:
ISBN 13: OCLC:632577030
Language: EN, FR, DE, ES & NL

Familial Mediterranean Fever in Children Book Review:

Familial Mediterranean Fever: New Insights for the Healthcare Professional: 2011 Edition

Familial Mediterranean Fever: New Insights for the Healthcare Professional: 2011 Edition
Author: Anonim
Publsiher: ScholarlyEditions
Total Pages: 21
Release: 2012-01-09
ISBN 10: 1464913285
ISBN 13: 9781464913280
Language: EN, FR, DE, ES & NL

Familial Mediterranean Fever: New Insights for the Healthcare Professional: 2011 Edition Book Review:

Familial Mediterranean Fever: New Insights for the Healthcare Professional: 2011 Edition is a ScholarlyPaper™ that delivers timely, authoritative, and intensively focused information about Familial Mediterranean Fever in a compact format. The editors have built Familial Mediterranean Fever: New Insights for the Healthcare Professional: 2011 Edition on the vast information databases of ScholarlyNews.™ You can expect the information about Familial Mediterranean Fever in this eBook to be deeper than what you can access anywhere else, as well as consistently reliable, authoritative, informed, and relevant. The content of Familial Mediterranean Fever: New Insights for the Healthcare Professional: 2011 Edition has been produced by the world’s leading scientists, engineers, analysts, research institutions, and companies. All of the content is from peer-reviewed sources, and all of it is written, assembled, and edited by the editors at ScholarlyEditions™ and available exclusively from us. You now have a source you can cite with authority, confidence, and credibility. More information is available at http://www.ScholarlyEditions.com/.

Increased Psoriasis Frequency in Patients with Familial Mediterranean Fever

Increased Psoriasis Frequency in Patients with Familial Mediterranean Fever
Author: Anonim
Publsiher: Anonim
Total Pages: 329
Release: 2018
ISBN 10:
ISBN 13: OCLC:1051853989
Language: EN, FR, DE, ES & NL

Increased Psoriasis Frequency in Patients with Familial Mediterranean Fever Book Review:

Abstract: Objective: Familial Mediterranean fever (FMF) is a periodic fever syndrome caused by MEFV mutations. FMF may be associated with psoriasis in some cases. The prevalence of psoriasis in the normal Turkish population is 0.42%. We aimed to investigate the prevalence of psoriasis among FMF patients and their relatives. Methods: FMF patients followed at Hacettepe University Adult and Pediatric Rheumatology Departments between January and August 2016 were included. FMF patients/their relatives were accepted to have psoriasis if the diagnosis was made by a dermatologist. Results: A total of 351 FMF patients (177 adults; 174 children) were included. The median (min–max) age of adult and pediatric patients was 35 (19–63) and 10 (2–18) years, respectively. Thirteen (3.7%) FMF patients (11 adults, 2 children) had psoriasis. Psoriasis was more common in adult than pediatric patients ( p = 0.02). Psoriasis was present in 22 (12.4%) of adult and 9 (5.2%) of pediatric patients' relatives ( p = 0.023). The frequency of psoriasis in ≥1 relatives of FMF patients was found to be 8.8%. Abdominal pain and fever were significantly higher, and arthralgia, arthritis, pleural chest pain, and pericarditis were significantly less frequent in the pediatric group than in adults ( p

Familial Mediterranean Fever

Familial Mediterranean Fever
Author: Marco Gattorno
Publsiher: Springer
Total Pages: 162
Release: 2015-03-19
ISBN 10: 3319146157
ISBN 13: 9783319146157
Language: EN, FR, DE, ES & NL

Familial Mediterranean Fever Book Review:

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.

Familial Mediterranean fever in children and adolescents: factors for colchicine dosage and predicting parameters for dose increase

Familial Mediterranean fever in children and adolescents: factors for colchicine dosage and predicting parameters for dose increase
Author: Anne-Marie Knieper
Publsiher: Anonim
Total Pages: 329
Release: 2018
ISBN 10:
ISBN 13: OCLC:1079408594
Language: EN, FR, DE, ES & NL

Familial Mediterranean fever in children and adolescents: factors for colchicine dosage and predicting parameters for dose increase Book Review:

A 44‐Year‐Old Female with Familial Mediterranean Fever, Cardiomyopathy and End Stage Renal Disease

A 44‐Year‐Old Female with Familial Mediterranean Fever, Cardiomyopathy and End Stage Renal Disease
Author: Anonim
Publsiher: Anonim
Total Pages: 329
Release: 2017
ISBN 10:
ISBN 13: OCLC:1051800331
Language: EN, FR, DE, ES & NL

A 44‐Year‐Old Female with Familial Mediterranean Fever, Cardiomyopathy and End Stage Renal Disease Book Review:

30 Day Journal & Tracker

30 Day Journal & Tracker
Author: Health Formation
Publsiher: Anonim
Total Pages: 62
Release: 2020-01-06
ISBN 10: 9781656468222
ISBN 13: 1656468220
Language: EN, FR, DE, ES & NL

30 Day Journal & Tracker Book Review:

After relentlessly studying the teachings of legendary healers, such as Dr Arnold Ehret and Dr Robert Morse, we set out on a journey of healing ourselves and reversing our very own conditions. Within our group, we were suffering from a range of diverse diseases and conditions, including Heart Disease, Kidney Disease, Diabetes, a variety of Autoimmune Diseases and Leaky Gut. During our healing journeys, we formed a journal that we would use on a daily basis, and this helped us to incorporate all of the lessons and tips that we had learnt and refined along the way - in short, it acted as a check list. It was important to us to not miss out on any knowledge and practices that had served us well. This journal is designed to guide and support you through your own journey with the core healing protocols included within its theme. One of the key conclusions that we reached through our individual journeys was that whether you are a sufferer of Familial Mediterranean Fever Autosomal Dominant, or any other condition, the same protocol that we used applies. However, dependant on the severity of your Familial Mediterranean Fever Autosomal Dominant, you may need to follow the protocols for longer, using specific herbs in order to achieve positive results, but you can make your own adjustments as you learn more. The great news is that all information and resources are readily available for personal study and application. Dr Arnold Ehret's books can be downloaded freely if you search for "arnold ehret books pdf". Visit rawfigs.com for Dr Robert Morse videos which can be searched through by keywords via the search bar. With this journal and your newly acquired knowledge, we trust that you will also soon start to experience the positive results that we did, along with the many others that send us regular positive feedback. We wish you all the best. The Health Formation Team

NORD Guide to Rare Disorders

NORD Guide to Rare Disorders
Author: National Organization for Rare Disorders
Publsiher: Lippincott Williams & Wilkins
Total Pages: 895
Release: 2003
ISBN 10: 9780781730631
ISBN 13: 0781730635
Language: EN, FR, DE, ES & NL

NORD Guide to Rare Disorders Book Review:

NORD Guide to Rare Disorders is a comprehensive, practical, authoritative guide to the diagnosis and management of more than 800 rare diseases. The diseases are discussed in a uniform, easy-to-follow format--a brief description, signs and symptoms, etiology, related disorders, epidemiology, standard treatment, investigational treatment, resources, and references.The book includes a complete directory of orphan drugs, a full-color atlas of visual diagnostic signs, and a Master Resource List of support groups and helpful organizations. An index of symptoms and key words offers physicians valuable assistance in finding the information they need quickly.

Familial Mediterranean Fever

Familial Mediterranean Fever
Author: Marco Gattorno
Publsiher: Springer
Total Pages: 162
Release: 2015-03-19
ISBN 10: 3319146157
ISBN 13: 9783319146157
Language: EN, FR, DE, ES & NL

Familial Mediterranean Fever Book Review:

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.

Familial Mediterranean Fever: New Insights for the Healthcare Professional: 2012 Edition

Familial Mediterranean Fever: New Insights for the Healthcare Professional: 2012 Edition
Author: Anonim
Publsiher: ScholarlyEditions
Total Pages: 29
Release: 2012-12-10
ISBN 10: 1464978921
ISBN 13: 9781464978920
Language: EN, FR, DE, ES & NL

Familial Mediterranean Fever: New Insights for the Healthcare Professional: 2012 Edition Book Review:

Familial Mediterranean Fever: New Insights for the Healthcare Professional / 2012 Edition is a ScholarlyPaper™ that delivers timely, authoritative, and intensively focused information about Familial Mediterranean Fever in a compact format. The editors have built Familial Mediterranean Fever: New Insights for the Healthcare Professional / 2012 Edition on the vast information databases of ScholarlyNews.™ You can expect the information about Familial Mediterranean Fever in this eBook to be deeper than what you can access anywhere else, as well as consistently reliable, authoritative, informed, and relevant. The content of Familial Mediterranean Fever: New Insights for the Healthcare Professional / 2012 Edition has been produced by the world’s leading scientists, engineers, analysts, research institutions, and companies. All of the content is from peer-reviewed sources, and all of it is written, assembled, and edited by the editors at ScholarlyEditions™ and available exclusively from us. You now have a source you can cite with authority, confidence, and credibility. More information is available at http://www.ScholarlyEditions.com/.

Syndromes: Rapid Recognition and Perioperative Implications

Syndromes: Rapid Recognition and Perioperative Implications
Author: Bruno Bissonnette,Igor Luginbuehl,Bernard J. Dalens,Bruno Marciniak
Publsiher: McGraw-Hill Education / Medical
Total Pages: 953
Release: 2006-08-10
ISBN 10:
ISBN 13: UOM:39015064795670
Language: EN, FR, DE, ES & NL

Syndromes: Rapid Recognition and Perioperative Implications Book Review:

Offers an A-Z encyclopedic presentation of more than 2000 syndromes. Each entry gives an overview of the syndrome, its major characteristics, genetic inheritance, pathophysiology, diagnosis, and clinical features. The overview provides access to the information needed to provide care for children and adults affected with pre-existing medical conditions.

Textbook of Autoinflammation

Textbook of Autoinflammation
Author: Philip J. Hashkes,Ronald M. Laxer,Anna Simon
Publsiher: Springer
Total Pages: 820
Release: 2019-02-13
ISBN 10: 3319986058
ISBN 13: 9783319986050
Language: EN, FR, DE, ES & NL

Textbook of Autoinflammation Book Review:

This book, the first complete textbook on this novel field in Medicine, comprehensively covers the clinical presentation, pathogenesis, genetics, and latest management strategies for autoinflammatory disorders as well as the basic science of autoinflammation. Relevant concepts such as how translational science of genetics and immunology relates to the innate immune system and autoinflammation are covered. Descriptions of the monogenic and polygenic/complex diseases that fall under the umbrella of autoinflammatory diseases are provided. Further topics covered include the latest clinical and genetic diagnostic approaches, concepts on the relationship between autoinflammation and autoimmunity/immunodeficiency, the role of autoinflammation in cancer, treatments and management strategies for these diseases, and potential areas of future development. The Textbook of Autoinflammation systematically describes and reviews diagnostic and treatment options for autoinflammatory disorders as well as all aspects of the concept of autoinflammation, and represents a valuable resource for professionals in a variety of disciplines who encounter these patients or who study autoinflammation.

Reversing Familial Mediterranean Fever

Reversing Familial Mediterranean Fever
Author: Health Central
Publsiher: Raw Power
Total Pages: 106
Release: 2019
ISBN 10: 9781395287986
ISBN 13: 1395287988
Language: EN, FR, DE, ES & NL

Reversing Familial Mediterranean Fever Book Review:

A truly resourceful and supporting workbook which will help you reach your health goals in a short space of time. A Must Have!

Familial Mediterranean Fever

Familial Mediterranean Fever
Author: Anonim
Publsiher: Anonim
Total Pages: 329
Release: 2016
ISBN 10:
ISBN 13: OCLC:1051324251
Language: EN, FR, DE, ES & NL

Familial Mediterranean Fever Book Review:

Abstract : Purpose of review: Familial Mediterranean fever (FMF) is the oldest and most common of the hereditary autoinflammatory diseases (AIDs). A large body of information has been accumulated over recent years on the pathophysiology, diagnosis and treatment of these diseases. The purpose of this review is to bring an up-to-date summary of the clinic manifestations, diagnostic criteria and treatment of FMF. Recent findings: An overview of the pathophysiologic basis of FMF as part of the AID is discussed. Over the last year, attempts to establish new criteria for childhood FMF, new guidelines for treatment and follow-up of disease and novel treatment for FMF were made. A comparison of the different disease severity scores for research purposes suggests that a new score is needed. New evidence for antiinterleukin-1 blockade as a new treatment modality is described. Summary: New diagnostic criteria, disease severity score, treatment and follow-up guidelines have been proposed, and need validation in the next several years.

The Heart in Rheumatic, Autoimmune and Inflammatory Diseases

The Heart in Rheumatic, Autoimmune and Inflammatory Diseases
Author: Udi Nussinovitch
Publsiher: Academic Press
Total Pages: 766
Release: 2017-02-10
ISBN 10: 0128032685
ISBN 13: 9780128032688
Language: EN, FR, DE, ES & NL

The Heart in Rheumatic, Autoimmune and Inflammatory Diseases Book Review:

The prevalence of autoimmune diseases and rheumatic conditions is constantly increasing. Autoimmune diseases affect approximately 7-10% of the population of the United States, while more than 50,000,000 American adults suffer from some type of arthritis. The Heart in Rheumatic, Autoimmune and Inflammatory Diseases examines the complex mechanisms relating to cardiac diseases from a pathophysiological and clinical point of view. Autoimmune rheumatic diseases can affect the coronary vessels, myocardium, pericardium, heart valves and the conduction system. The diagnosis of these unique cardiac complications necessitates medical awareness and a high index of suspicion. Increased risk of advanced atherosclerosis plays a pivotal role in the development of cardiac diseases in systemic, rheumatic and autoimmune illnesses. Yet, other complex immune medicated mechanisms may contribute to the pathogenesis. Patients' optimal care requires coordination between the primary caregiver, the rheumatologist, immunologist and cardiologist. Screening for cardiovascular risk factors, recognition of high-risk patients and identification of subclinical cardiac conditions are of great importance. Moreover, regulation of inflammation, as well as abnormal immune responses and the initiation of early treatments should be the focus of patient management. A continuous attempt to identify novel therapeutic targets and change the natural history of the underlying disease and its cardiac manifestations is in progress. The book aims at providing the readers with a state of the art collection of up to date information regarding clinically important topics based on experts' perspectives. This book was a result of an extended coordinated collaboration of one-hundred and fifty-four distinguished scientists from thirty-one countries around the globe. A review of common, as well as unusual (yet clinically significant) medical cardiac complications of prevalent rheumatic, autoimmune and inflammatory diseases. Focuses on aspects of pathophysiological processes, clinical presentations, screening tests, prognostic implications and novel therapeutic approaches. Presents an up-to-date “level of evidence and “strengths of recommendations for suggested therapies and reviews all randomized clinical trials, meta-analyses and other supporting published clinical findings.

Commentaries on the History and Cure of Diseases

Commentaries on the History and Cure of Diseases
Author: William Heberden
Publsiher: Anonim
Total Pages: 431
Release: 1816
ISBN 10:
ISBN 13: UOM:39015071040391
Language: EN, FR, DE, ES & NL

Commentaries on the History and Cure of Diseases Book Review:

Ischemia-Modified Albumin and Atherosclerosis in Patients With Familial Mediterranean Fever

Ischemia-Modified Albumin and Atherosclerosis in Patients With Familial Mediterranean Fever
Author: Anonim
Publsiher: Anonim
Total Pages: 329
Release: 2016
ISBN 10:
ISBN 13: OCLC:1053726813
Language: EN, FR, DE, ES & NL

Ischemia-Modified Albumin and Atherosclerosis in Patients With Familial Mediterranean Fever Book Review:

The constriction of vessels due to atherosclerotic lesions causes hypoxia/ischemia and oxidative changes resulting in transformation of free albumin to ischemia-modified albumin (IMA) in the circulation and increased carotid intima–media thickness (cIMT). We investigated the reliability of IMA increase in evaluating atherosclerosis in patients with familial Mediterranean fever (FMF) compared with cIMT. Patients with FMF (n = 58) diagnosed by the Tel-Hashomer criteria in attack-free period and 38 healthy people were included in the study. Patient demographics as well as the clinical and laboratory characteristics of the healthy controls and patients with FMF were noted. The IMA levels and cIMT in patients with FMF were 0.30 ± 0.09 absorbance units (ABSUs) and 1.12 ± 0.27 mm, respectively, and in the control group, IMA levels and cIMT were 0.25 ± 0.07 ABSU and 0.74 ± 0.26 mm, respectively. The IMA levels and cIMT were significantly higher in patients with FMF than in controls ( P = .020 and P

Auto-Inflammatory Syndromes

Auto-Inflammatory Syndromes
Author: Petros Efthimiou
Publsiher: Springer
Total Pages: 322
Release: 2019-01-04
ISBN 10: 3319969293
ISBN 13: 9783319969299
Language: EN, FR, DE, ES & NL

Auto-Inflammatory Syndromes Book Review:

This book provides an overview of auto-inflammatory syndromes, covering the underlying immune mechanisms that lead to their development, specific disease presentations, and clinical treatment guidelines. The book is divided into two sections, adult and pediatric, with chapters focusing on individuals diseases such as systemic arthritis, hyper-IgD, pap syndrome, idiopathic recurrent pericarditis, and familial Mediterranean fever. Chapters incorporate the most recent advances in disease pathophysiology and examine the underlying inductive and effector mechanisms and therapies that relate to each auto-inflammatory disorder at the genetic, molecular, cellular, and epidemiologic levels. The book also discusses the research behind auto-inflammatory disorders to offer detailed clinical guidelines regarding diagnostic techniques, treatment plans, and advice on how to best transition pediatric patients into adult treatment. This is an invaluable reference on auto-inflammatory syndromes for clinicians and researchers in pediatric and adult rheumatology and immunology.

Skin Manifestations in Rheumatic Disease

Skin Manifestations in Rheumatic Disease
Author: Marco Matucci-Cerinic,Daniel Furst,David Fiorentino
Publsiher: Springer Science & Business Media
Total Pages: 410
Release: 2013-09-11
ISBN 10: 1461478499
ISBN 13: 9781461478492
Language: EN, FR, DE, ES & NL

Skin Manifestations in Rheumatic Disease Book Review:

Rheumatologic diseases are highly associated with clinical symptoms of the skin, nails, and mucosal membranes. This book provides the practicing rheumatologist with a rapid, easy to consult reference to help interpret the nature of these cutaneous lesions and then quickly decide upon the appropriate follow-up tests. Utilizing an abundance of informative photographs, it contains all of the essential information needed for early diagnosis and treatment. This comprehensive guide properly orients the practitioner within the challenging world of rheumatologic disorders of the skin and gives insight into when consultation with a dermatologist is advisable.

Genetic Disorders Among Arab Populations

Genetic Disorders Among Arab Populations
Author: Ahmad S. Teebi
Publsiher: Springer Science & Business Media
Total Pages: 772
Release: 2010-07-30
ISBN 10: 9783642050800
ISBN 13: 3642050808
Language: EN, FR, DE, ES & NL

Genetic Disorders Among Arab Populations Book Review:

Arab populations have their “own” genetic disorders, both universal and particular. Genetic diversity within these source populations, along with the fact that the rates of inbreeding are often high and family sizes are often large, constitute conditions that facilitate the emergence and detection of phenotypes explained notably by autosomal recessive inheritance; in which case, the use of homozygosity gene mapping can facilitate the discovery of the corresponding genes. The present book includes 5 parts dealing with various aspects that relate to the genetic structure of Arabs and minorities within the Arab world as well as genetic disorders prevalent in this part of the world. It includes updated reviews of the genetic disorders in various Arab countries and geographic regions. The focus is primarily, but not exclusively, on the group of single-gene disorders with particular emphasis on autosomal recessive conditions. It further includes epidemiological and clinical data as well as inheritance patterns, mutation and polymorphism data, and available haplotype analysis data. The ethnic and genetic diversity of the Arab populations is discussed as well as aspects of genetic counseling practice in this region together with a proposal for an ethical framework for genetic research and prevention of genetic disorders. The target audience of this book includes human and medical geneticists, genetic counselors, researchers, medical specialists dealing with Arab patients or practicing in Arab countries, medical and genetic counseling students, and nurses.