نتایج جستجو برای: primary immunodeficiency disease

تعداد نتایج: 2088150  

Journal: :acta medica iranica 0
zinat nadia hatmi department of community medicine, tehran university of medical sciences, tehran ,iran. mitra mahdavi-mazdeh department of nephrology, tehran university of medical sciences, tehran ,iran. seyed saeid hashemi-nazari health city office, tehran municipality, tehran ,iran. ebrahim hajighasemi health city office, tehran municipality, tehran ,iran. behnaz nozari research center of iranian tissue bank, tehran, iran. azita mahdavi national behzisti organization, tehran, iran.

more than eighty percent of patients with coronary heart diseases (chd) have conventional risk factors. prevalence of well known risk factors seems to show a different pattern in younger patients and individual above 55 years. to evaluate the pattern of conventional chd risk factors in healthy individuals in two different age groups. a large scale population based survey of 31999 individuals fr...

Journal: :Indian pediatrics 1992
M Salaria S Singh L Kumar

Hyperimmunoglobulin E (HIE) syndrome is a primary immunodeficiency disorder characterized by recurrent bacterial infections in presence of very high serum Ig E levels. We are reporting a nine-year-old child with HIE syndrome and reviewing literature on this disease.

2009
KATERINA SALAVOURA AGGELIKI KOLIALEXI GEORGE TSANGARIS ARIADNI MAVROU

Primary immunodeficiencies (PIDs) are genetic disorders that predispose to frequent and severe infections, autoimmunity and cancer. The expanded life span of such patients increases the overall risk for developing cancer, which is now estimated at 4-25% . The type of malignancy depends on the primary immunodeficiency, the age of the patient and possible viral infection, suggesting that differen...

2013
Jonathan S. Tam John M. Routes

Common variable immunodeficiency (CVID) is a common primary immunodeficiency characterized by a failure in B-cell differentiation with defective immunoglobulin production. Affected patients are uniquely susceptible to recurrent infection with encapsulated organisms and have an increased propensity for the development of inflammatory and autoimmune manifestations. The diagnosis of CVID is common...

Journal: :The Yale Journal of Biology and Medicine 1984
Robert S. Baltimore

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...

Journal: :Revista espanola de enfermedades digestivas : organo oficial de la Sociedad Espanola de Patologia Digestiva 2013
Juan María Vázquez-Morón Héctor Pallarés-Manrique Ignacio Javier Martín-Suárez Beatriz Benítez-Rodríguez Manuel Ramos-Lora

Common variable immunodeficiency (CVID) is the most frequent primary antibody deficiency. It is characterized by recurrent bacterial infections, and occurrence of autoimmune and neoplastic diseases is also frequent; there is also a high prevalence of gastrointestinal diseases. There are reports of inflammatory bowel disease in this entity, but incidence is low (2-4 %). We present the case of a ...

Journal: : 2023

The article presents a clinical case of rare primary immunodeficiency syndrome Hyperimmunoglobulinemia E. Typical symptoms, diagnostic and treatment tactics have been demonstrated.

Journal: :Journal of investigational allergology & clinical immunology 2008
A Fahimzad Z Chavoshzadeh H Abdollahpour C Klein N Rezaei

Severe congenital neutropenia (SCN) is a primary immunodeficiency disease characterized by early onset of severe bacterial infection and persistent severe neutropenia. We describe an SCN patient with a history of recurrent infections. The clinical course was complicated by necrosis of the nasal cartilage due to mucormycosis. Molecular studies revealed a homozygous germline HAX1 mutation. Fungal...

Journal: :BMJ 1989
I C Macdougall R D Hutton I Cavill G A Coles J D Williams

human immunodeficiency virus infection in haemophiliacs. Lancet 1986;ii: 1233-6. 12 Centers for Disease Control. Classification system for human T-lymphotropic virus type Illymphadenopathy-associated virus infections. Ann Intern Med 1986;105:234-7. 13 Centers for Disease Control. Revision of the case definition of acquired immunodeficiency syndrome for national reporting. MMWR 1985;34: 374-5. 1...

2015
MM Esser

Selective IgA deficiency (IgAD) is the most common primary genetic immune defect, with high prevalence in Western countries and relatively low prevalence in the East. The laboratory definition of IgAD is based on the measured serum component. However, the important manifestations of deficiency of IgA, the most prevalent of human antibodies, relate to the absence of secretory IgA, which covers a...

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