Fibrinogen A alpha-chain associated amyloidosis: Difference between revisions
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==Pathophysiology== | ==Pathophysiology== | ||
Fibrinogen is a plasma protein with a crucial role in the coagulation cascade through its conversion to fibrin | |||
It is composed of 2 identical sets of 3 polypeptide chains termed A α, B β, and γ, joined by disulfide bridging. | |||
Each polypeptide is encoded by a distinct gene, FGA, FGB, and FGG. | |||
The gene for the fibrinogen A α-chain with 610 amino acid residues is localized on chromosome 4 and has 6 exons. | |||
Mutations in any of the 3 genes encoding for fibrinogen polypeptides can cause dysfibrinogenemias | |||
Recently identified mutations in the A α-chain gene can lead to hereditary systemic amyloidosis | |||
==Causes== | ==Causes== |
Revision as of 23:41, 5 November 2019
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief:
Synonyms and keywords:Fibrinogen amyloidosis
Overview
Historical Perspective
Fibrinogen amyloidosis was first discovered by Dr Merill Benson et al, an American physician, in 1993.[1]
Classification
Pathophysiology
Fibrinogen is a plasma protein with a crucial role in the coagulation cascade through its conversion to fibrin
It is composed of 2 identical sets of 3 polypeptide chains termed A α, B β, and γ, joined by disulfide bridging.
Each polypeptide is encoded by a distinct gene, FGA, FGB, and FGG.
The gene for the fibrinogen A α-chain with 610 amino acid residues is localized on chromosome 4 and has 6 exons.
Mutations in any of the 3 genes encoding for fibrinogen polypeptides can cause dysfibrinogenemias
Recently identified mutations in the A α-chain gene can lead to hereditary systemic amyloidosis
Causes
Epidemiology and Demographics
is emerging as the most common type of all hereditary renal amyloid diseases in the United Kingdom and Europe.
A tertiary US amyloid reference center suggestsfibrinogen A alpha-chain amyloidosis is the leading cause of hereditary renal amyloidosis associated with nephrotic syndrome in the United States.
Risk Factors
Screening
Natural History, Complications, and Prognosis
Diagnosis
Diagnostic Study of Choice
History and Symptoms
Physical Examination
Laboratory Findings
Electrocardiogram
X-ray
Echocardiography or Ultrasound
CT scan
MRI
Other Imaging Findings
Other Diagnostic Studies
Treatment
Medical Therapy
Fibrinogen production is exclusively hepatic. Isolated renal transplantation as a treatment for renal failure in fibrinogen amyloidosis is of limited value.[2]
Surgery
Primary Prevention
Secondary Prevention
References
- ↑ Benson MD, Liepnieks J, Uemichi T, Wheeler G, Correa R (1993). "Hereditary renal amyloidosis associated with a mutant fibrinogen alpha-chain". Nat Genet. 3 (3): 252–5. doi:10.1038/ng0393-252. PMID 8097946.
- ↑ Mousson C, Heyd B, Justrabo E, Rebibou JM, Tanter Y, Miguet JP; et al. (2006). "Successful hepatorenal transplantation in hereditary amyloidosis caused by a frame-shift mutation in fibrinogen Aalpha-chain gene". Am J Transplant. 6 (3): 632–5. doi:10.1111/j.1600-6143.2005.01199.x. PMID 16468976.