Hypogammaglobulinemia: Difference between revisions

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Hypogammaglobulinemia is a characteristic of [[common variable immunodeficiency]].<ref>{{DorlandsDict|four/000052585|common variable immunodeficiency}}</ref>
Hypogammaglobulinemia is a characteristic of [[common variable immunodeficiency]].<ref>{{DorlandsDict|four/000052585|common variable immunodeficiency}}</ref>
==Terminology==
"Hypogammaglobulinemia" is largely synonymous with "agammaglobulinemia". When the latter term is used (as in "[[X-linked agammaglobulinemia]]") it implies that gamma globulins are not merely reduced, but completely absent. Modern assays have allowed most agammaglobulinemias to be more precisely defined as hypogammaglobulinemias,<ref>{{DorlandsDict|one/000002160|agammaglobulinemia}}</ref> but the distinction is not usually clinically relevant.
"Hypogammaglobulinemia" is largely synonymous with "agammaglobulinemia". When the latter term is used (as in "[[X-linked agammaglobulinemia]]") it implies that gamma globulins are not merely reduced, but completely absent. Modern assays have allowed most agammaglobulinemias to be more precisely defined as hypogammaglobulinemias,<ref>{{DorlandsDict|one/000002160|agammaglobulinemia}}</ref> but the distinction is not usually clinically relevant.


"Hypogammaglobulinemia" is distinguished from [[dysgammaglobulinemia]], which is a reduction in some types of [[gamma globulin]]s, but not others.<ref>{{DorlandsDict|three/000033050|Dysgammaglobulinemia}}</ref>
"Hypogammaglobulinemia" is distinguished from [[dysgammaglobulinemia]], which is a reduction in some types of [[gamma globulin]]s, but not others.<ref>{{DorlandsDict|three/000033050|Dysgammaglobulinemia}}</ref>


==Types==
==Historical Perspective==
 
==Classification==
{| class="wikitable"
{| class="wikitable"
|-
|-
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==References==
==Pathophysiology==
{{reflist|2}}
 
==Causes==
 
==Differentiating {{PAGENAME}} from Other Diseases==
 
==Epidemiology and Demographics==
 
==Risk Factors==
 
==Screening==
 
==Natural History, Complications, and Prognosis==
===Natural History===
 
===Complications===
 
===Prognosis===
 
==Diagnosis==
===Diagnostic Criteria===
 
===History and Symptoms===
 
===Physical Examination===
 
===Laboratory Findings===
 
===Imaging Findings===
 
===Other Diagnostic Studies===
 
==Treatment==
===Medical Therapy===
 
===Surgery===
 
===Prevention===


==External links==
==External links==
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* Robert Y Li, et al.: "[http://emedicine.medscape.com/article/136471-overview Hypogammaglobulinemia]", ''Medscape''. Accessed 2009-07-17.
* Robert Y Li, et al.: "[http://emedicine.medscape.com/article/136471-overview Hypogammaglobulinemia]", ''Medscape''. Accessed 2009-07-17.
* Saul Greenberg: "[http://www.utoronto.ca/kids/Hypogam.htm Hypogammaglobulinemia ]". Accessed 2009-07-17.
* Saul Greenberg: "[http://www.utoronto.ca/kids/Hypogam.htm Hypogammaglobulinemia ]". Accessed 2009-07-17.
==References==
{{reflist|2}}
{{WS}}
{{WH}}


{{Immune disorders}}
{{Immune disorders}}
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{{Cell surface receptor deficiencies}}
{{Cell surface receptor deficiencies}}


[[Category:Lymphocytic immune system disorders]]
[[Category:Immunology]]
[[Category:Hematology]]

Revision as of 15:35, 23 June 2016

Hypogammaglobulinemia
ICD-10 D80.0-D80.1
ICD-9 279.00
DiseasesDB 6426
MedlinePlus 001307
eMedicine med/1120  ped/54
MeSH D000361

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List of terms related to Hypogammaglobulinemia

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]

Overview

Hypogammaglobulinemia is a type of primary immune deficiency disease.[1]

Hypogammaglobulinemia is a characteristic of common variable immunodeficiency.[2] "Hypogammaglobulinemia" is largely synonymous with "agammaglobulinemia". When the latter term is used (as in "X-linked agammaglobulinemia") it implies that gamma globulins are not merely reduced, but completely absent. Modern assays have allowed most agammaglobulinemias to be more precisely defined as hypogammaglobulinemias,[3] but the distinction is not usually clinically relevant.

"Hypogammaglobulinemia" is distinguished from dysgammaglobulinemia, which is a reduction in some types of gamma globulins, but not others.[4]

Historical Perspective

Classification

Type OMIM Gene
AGM1 601495 IGHM
AGM2 613500 IGLL1
AGM3 613501 CD79A
AGM4 613502 BLNK
AGM5 613506 LRRC8A
AGM6 612692 CD79B

Pathophysiology

Causes

Differentiating Hypogammaglobulinemia from Other Diseases

Epidemiology and Demographics

Risk Factors

Screening

Natural History, Complications, and Prognosis

Natural History

Complications

Prognosis

Diagnosis

Diagnostic Criteria

History and Symptoms

Physical Examination

Laboratory Findings

Imaging Findings

Other Diagnostic Studies

Treatment

Medical Therapy

Surgery

Prevention

External links

  • Template:DorlandsDict
  • Rose, M. E.; Lang, D. M. (2006). "Evaluating and managing hypogammaglobulinemia". Cleveland Clinic journal of medicine. 73 (2): 133–7, 140, 143–4. PMID 16478038.
  • Robert Y Li, et al.: "Hypogammaglobulinemia", Medscape. Accessed 2009-07-17.
  • Saul Greenberg: "Hypogammaglobulinemia ". Accessed 2009-07-17.

References

Template:WS Template:WH

Template:Disorders of globin and globulin proteins Template:Cell surface receptor deficiencies