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139:- Selective immunoglobulin A deficiency is classified as an IgA level below 7mg/dl (0.4375 ÎĽmol/L) with normal levels of other immunoglobulins. Some people with selective immunoglobulin A deficiency are prone to infections and develop other autoimmune disorders such as lupus, celiac disease and inflammatory bowel disease while others are completely asymptomatic.
155:- IgG deficiency is a lack of IgG in the absence of other immunoglobulin deficiencies. IgG levels of 300–600 mg/dL show a mild to moderate reduction of IgG while levels below 200 mg/dl are classified as a severe deficiency. Those with IgG deficiency often get chronic or reoccurring pyogenic respiratory tract infections.
147:- Selective IgE deficiency disease is characterized by IgE levels below <2 kIU/L with normal levels of other immunoglobulins. Selective IgE deficiency disease may be associated with an increased predisposition to certain sinopulmonary diseases, autoimmune disorders, infections, and malignancies.
519:
Cheraghi, Taher; Kalantari, Arash; Shabestari, Mahnaz
Sadeghi; Abolhassani, Hassan; Eibel, Hermann; Hammarström, Lennart; Kanegane, Hirokazu; Durandy, Anne; Plebani, Alessandro; Cunningham-Rundles, Charlotte; Aghamohammadi, Asghar (2021). "Predominantly antibody deficiencies".
163:- Isolated primary immunoglobulin M deficiency is classified as IgM levels under two SD of mean with normal levels of other immunoglobulins. Isolated primary immunoglobulin M deficiency often presents as recurring infections. Patients often improve with immunoglobulin therapy.
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Magen, Eli; Schlesinger, Menachem; David, Michael; Ben-Zion, Itzhak; Vardy, Daniel (March 1, 2014).
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van der Burg, Mirjam; Dalm, Virgil A.S.H.; Weemaes, Corry M.R. (2020). "Isotype defects".
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432:"Immunoglobulin G Deficiency Clinical Presentation: History, Physical, Causes"
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458:"Selective IgM Deficiency—An Underestimated Primary Immunodeficiency"
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320:"Selective IgE deficiency, immune dysregulation, and autoimmunity"
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373:"Assessment and clinical interpretation of reduced IgG values"
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Agarwal, Shradha; Cunningham-Rundles, Charlotte (2007).
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Gupta, Sudhir; Gupta, Ankmalika (September 5, 2017).
271:(1). Springer Science and Business Media LLC: 10–16.
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127:There are four main types of dysgammaglobulinemia.
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1176:Index of articles associated with the same name
667:Isolated primary immunoglobulin M deficiency:
109:characterized by a reduction in some types of
759:
8:
161:Isolated primary immunoglobulin M deficiency
94:Isolated primary immunoglobulin M deficiency
984:Purine nucleoside phosphorylase deficiency
832:Transient hypogammaglobulinemia of infancy
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377:Annals of Allergy, Asthma & Immunology
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330:(2). Oceanside Publications Inc.: 27–33.
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618:Selective immunoglobulin A deficiency:
190:
39:Schematic diagram of the basic unit of
1148:Terminal complement pathway deficiency
137:Selective immunoglobulin A deficiency
86:Selective immunoglobulin A deficiency
7:
430:Schwartz, Robert A (June 30, 2023).
88:, Selective IgE deficiency disease,
1209:Predominantly antibody deficiencies
1153:Paroxysmal nocturnal hemoglobinuria
638:Selective IgE deficiency disease:
567:10.1016/b978-0-12-816768-7.00020-x
532:10.1016/b978-0-12-821028-4.00006-3
14:
54:dis-gam″ә-glob″u-lin-e´me-ә
1169:
916:Common variable immunodeficiency
145:Selective IgE deficiency disease
1088:Idiopathic CD4+ lymphocytopenia
1158:Complement receptor deficiency
1028:Adenosine deaminase deficiency
324:Allergy and Asthma Proceedings
265:Journal of Clinical Immunology
1:
390:10.1016/s1081-1206(10)60665-5
672:Immune Deficiency Foundation
612:Dorland's Medical Dictionary
558:Stiehm's Immune Deficiencies
468:. Frontiers Media SA: 1056.
223:Dorland's Medical Dictionary
206:Dorland's Medical Dictionary
827:X-linked agammaglobulinemia
383:(3). Elsevier BV: 281–283.
1225:
1168:
261:"Selective IgA Deficiency"
124:types of gamma globulins.
120:, which is a reduction in
523:Inborn Errors of Immunity
278:10.1007/s10875-009-9357-x
116:It is distinguished from
38:
29:
1043:Bare lymphocyte syndrome
895:Wiskott–Aldrich syndrome
475:10.3389/fimmu.2017.01056
336:10.2500/aap.2014.35.3734
1143:Complement 3 deficiency
1128:Complement 4 deficiency
1124:Complement 2 deficiency
462:Frontiers in Immunology
218:"hypogammaglobulinemia"
16:Type of immune disorder
604:Dysgammaglobulinemia:
201:"Dysgammaglobulinemia"
1118:Hereditary angioedema
974:Ataxia–telangiectasia
819:Hypogammaglobulinemia
240:monarchinitiative.org
179:Hypogammaglobulinemia
118:hypogammaglobulinemia
1138:Properdin deficiency
959:Di George's syndrome
842:Dysgammaglobulinemia
236:"Monarch Initiative"
103:Dysgammaglobulinemia
25:Dysgammaglobulinemia
259:Yel, Leman (2010).
1204:Set index articles
990:Hyper IgM syndrome
900:Hyper-IgE syndrome
865:Hyper IgM syndrome
781:disorders causing
640:Monarch Initiative
606:Monarch Initiative
436:Medscape Reference
1180:set index article
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950:thymic hypoplasia
935:T cell deficiency
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1038:ZAP70 deficiency
969:Nezelof syndrome
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643:Disease Ontology
620:Cleveland Clinic
609:Disease Ontology
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1080:Lymphocytopenia
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588:. Retrieved
561:. Elsevier.
557:
545:. Retrieved
526:. Elsevier.
522:
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441:November 27,
439:. Retrieved
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981:peripheral:
632:Mayo Clinic
623:MerckManual
1198:Categories
1114:Angioedema
1100:deficiency
1098:Complement
1075:Leukopenia
1025:autosomal:
779:complement
590:2023-11-27
547:2023-11-27
357:2023-11-27
245:2023-11-27
185:References
68:Hematology
43:(antibody)
1018:x-linked:
732:123782009
727:SNOMED CT
678:EMedicine
660:EMedicine
626:EMedicine
585:241231704
484:1664-3224
399:1081-1206
344:1088-5412
287:0271-9142
63:Specialty
1065:HIV/AIDS
1057:Acquired
1008:combined
800:Antibody
775:Lymphoid
675:UpToDate
663:UpToDate
502:28928736
417:17910333
352:24717782
305:20101521
168:See also
804:humoral
791:Primary
721:D004406
629:DermNet
493:5591887
408:3099256
296:2821513
1185:If an
1021:X-SCID
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909:Other
581:S2CID
131:Types
82:Types
777:and
716:MeSH
705:9-CM
669:GARD
571:ISBN
536:ISBN
498:PMID
480:ISSN
443:2023
413:PMID
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301:PMID
283:ISSN
701:ICD
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