C4 glomerulopathy: Difference between revisions

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{{C4 glomerulopathy}}                                                                 
{{C4 glomerulopathy}}                                                                 
{{CMG}}; {{APM}} {{AE}} {{OO}}
{{CMG}}; {{APM}} {{AE}} {{OO}} {{ Norina Usman}}
   
   
{{SK}} glomerulonephritis; C4 glomerulonephritis; dense deposit disease
{{SK}} glomerulonephritis; C4 glomerulonephritis; dense deposit disease
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==[[C4 glomerulopathy natural history|Natural History, Complications and Prognosis]]==
==[[C4 glomerulopathy natural history|Natural History, Complications and Prognosis]]==
If left untreated, C4 glomerulopathy may progress to develop renal failure.


==Diagnosis==
==Diagnosis==

Latest revision as of 03:27, 25 August 2020

C4 glomerulopathy Microchapters

Complement Mediated Glomerular Disorders Main Page

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Overview

Historical Perspective

Classification

Pathophysiology

Causes

Differentiating C4 glomerulopathy from other Diseases

Epidemiology and Demographics

Risk Factors

Screening

Natural History, Complications and Prognosis

Diagnosis

History and Symptoms

Physical Examination

Laboratory Findings

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CT

MRI

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Case #1

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Ali Poyan Mehr, M.D. [2] Associate Editor(s)-in-Chief: Olufunmilola Olubukola M.D.[3] Norina Usman, M.B.B.S[4]

Synonyms and keywords: glomerulonephritis; C4 glomerulonephritis; dense deposit disease

Overview

Historical Perspective

There is limited information about the historical perspective of C4 glomerulopathy.

Classification

C4 glomerulopathy may be classified based on complement deposition into Dense Deposit Disease (DDD) and C4 Glomerulonephritis (C4GN).

Pathophysiology

It is thought that C4 glomerulopathy is the result of the activation of immune complex glomerulonephritis or lectin pathway of the complement.

Causes

C4 glomerulopathy may be caused by mutation of complement factor,anti-factor H, anti-factor B, or C4 nephritic factor.

Differentiating C4 glomerulopathy from other Diseases

C4 glomerulopathy must be differentiated from other diseases that cause proteinuria, hematuria, and peripheral edema, such as IgA nephropathy, membranous nephropathy, focal segmental glomerulus /minimal change disease, membranoproliferative glomerulonephritis, and lupus nephritis.

Epidemiology and Demographics

There is not much information available about the incidence and prevalence.

Risk factors

There are no established risk factors for C4 glomerulopathy.

Screening

There is insufficient information to recommend routine screening for C4 glomerulopathy.

Natural History, Complications and Prognosis

If left untreated, C4 glomerulopathy may progress to develop renal failure.

Diagnosis

History and Symptoms | Physical Examination | Laboratory Findings | X ray | CT | MRI | Echocardiography or Ultrasound | Other Imaging Studies | Other Diagnostic Studies

Treatment

Surgery | Medical therapy | Primary Prevention | Secondary Prevention | Cost-Effectiveness of Therapy | Future or Investigational Therapies

Case Studies

Case #1

References

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