LUPUS ERYTHEMATEUX SYSTEMIQUE PDF

30 janv. Le lupus érythémateux systémique (ou lupus érythémateux disséminé), représente la forme la plus courante de lupus. Le terme «lupus», plus. Disease definition. Autosomal systemic lupus erythematosus is a rare, genetic, multisystemic, chronic autoimmune disease characterized by the presence of. LE LUPUS ERYTHEMATEUX SYSTEMIQUE: EXPÉRIENCE DU SERVICE DE MÉDECINE INTERNE CHU D’OUJDA (Apropos de 54 cas).

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[Seizures in patients with systemic lupus erythematosus].

Infectious complications were noted in Only comments written in English can be processed. Autosomal systemic lupus erythematosus is a rare, genetic, multisystemic, chronic autoimmune disease characterized by the presence of systemic lupus erythematosus symptoms in two or more members of a single family.

Summary and related texts. Check this box if you wish to receive a copy of your message. It predominantly affects young women of childbearing age and evolves in spurts.

Specialised Social Services Eurordis directory. Disease definition Autosomal systemic lupus erythematosus is a rare, genetic, multisystemic, chronic autoimmune disease characterized by the presence of systemic lupus erythematosus symptoms in two or more members of a single family.

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The female predominance is very clear in our series with an average age of For all other comments, please send your remarks via contact us.

The systemic lupus erythematosus is considered among the more leading non-specific organ autoimmune diseases understood, it is now well established that this disease results from the interaction of multiple genetic and environmental factors, leading to inappropriate activation of the immune system.

Renal and neurological prognosis dominate.

WHOART, French Translation – SYNDROME DE LUPUS ERYTHEMATEUX – Classes | NCBO BioPortal

Its prevalence varies from one country to another. It is characterized by a highly polymorphic systemic involvement and autoimmune response directed against nuclear antigens. Additional information Further information on this disease Classification s 3 Gene s 5 Other website s 1. Other search option s Alphabetical list.

Lupus – Causes, symptômes et traitement – Santé-Médecine

Only comments seeking to improve the quality and accuracy of information on the Orphanet website are accepted. Patients present a wide spectrum of clinical manifestations, including cutaneous malar rash, photosensitivityocular keratoconjunctivitis sicca, retinopathygastrointestinal oral ulceration, abdominal paincardiac atherosclerosis, chest painpulmonary serositis, pleurisymusculoskeletal arthralgia, myalgiarenal nephritis, hematuriaobstetrical increased spontaneous abortions, neonatal lupusconstitutional fatigue, loss of appetite and neuropsychiatric mood and cognitive disorders involvement, among others.

A single-center experience from Morocco. Health care resources for this disease Expert centres Diagnostic tests 1 Patient organisations 38 Orphan drug s 0. The problem of diagnosis delay was common in our series as well as selfmedication upstream of any clear diagnosis and complete set. These problems are not related to access to care but also to the lack of interest devoted to famous rare systemic diseases in our country and therefore not a priority, which is the source not only of diagnostic problem but also the great difficulty to support patients after the diagnosis carried out due to the high cost of care of such pathologies.

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The prognosis depends on the nature of visceral lesions.

Detailed information Article for general public Deutschpdf. The documents contained in this web site are presented for information purposes only.

The prevalence of major organ involvement were: The material is in no way intended to replace professional medical care by a qualified specialist and should not be used as a basis for diagnosis or treatment.