منابع مشابه
Importace of monoclonal immunoglobulin in Sjögren’s syndrome
Background: Sjögren’s syndrome is the second most common systemic autoimmune disease after rheumatoid arthritis, RA, with a prevalence of about 0.5% in the general population. It occurs primarily in perimenopausal women (at a ratio of women to men of 9: 1) Sjögren’s syndrome is characterized by lymphocytic infiltration to exocrine glands. The specific autoantibodies of this syndrome are against...
متن کاملSpecific polysaccharide antibody deficiency in chromosome 18p deletion syndrome and immunoglobulin A deficiency.
Immunoglobulin (Ig) A deficiency has long been recognized in patients with chromosome 18 abnormalities. We present the case of a young girl in whom a chromosome 18p deletion syndrome (46,XX,del[18][p11.1]) was associated not only with IgA deficiency, but also with an inability to make antibody to the unconjugated pneumococcal polysaccharide vaccine, Pneumovax II, indicating a concomitant specif...
متن کاملGranulomatous gastritis, iron deficiency, vitamin B12 malabsorption and immunoglobulin deficiency.
ODEBURG, B. (1965) Eosinophilic leukaemia and disseminated eosinophilic collagen disease-a disease entity? Acta medica scandinavica, 177, 129. PHILLIPS, P.E. & CHRISTIAN, C.L. (1973) Virus antibodies in SLE and other connective tissue diseases. Annals of the Rheumatic Diseases, 32, 480. PIERCE, L.E., HOSSEINIAN, A.H. & CONSTANTINE, A.B. (1967) Disseminated eosinophilic collagen disease. Blood, ...
متن کاملImmunoglobulin treatment in primary antibody deficiency.
The primary antibody deficiency syndromes are characterised by recurrent respiratory tract infections and the inability to produce effective immunoglobulin (Ig) responses. The best-known primary antibody deficiencies are common variable immunodeficiency (CVID), X-linked agammaglobulinaemia (XLA), immunoglobulin G (IgG) subclass deficiency, and selective antibody deficiency with normal immunoglo...
متن کاملPrimary immunoglobulin deficiency and haematological disorders.
Nine patients with immunoglobulin deficiency and various haematological disorders are presented. In all patients, recurrent infections had antedated the onset of the haematological disorder but, in most, the possibility of primary immunodeficiency had not been considered until after the haematological diagnosis had been established. The recognition of immunodeficiency is important since such pa...
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ژورنال
عنوان ژورنال: BMJ
سال: 1973
ISSN: 0959-8138,1468-5833
DOI: 10.1136/bmj.1.5855.743-a