Familial amyloidosis classification: Difference between revisions
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{{familytree | | B10 | | B11 | | B12 | | B13 | | B14 | | B15 | | B16 |B10='''Transthyretin (TTR)'''|B11='''Apolipoprotein AI'''|B12='''Gelsolin'''|B13='''Lysozyme'''|B14='''Cystatin C'''|B15='''Fibrinogen Aa-chain'''|B16='''Apolipoprotein AII'''}} | {{familytree | | B10 | | B11 | | B12 | | B13 | | B14 | | B15 | | B16 |B10='''Transthyretin (TTR)'''|B11='''Apolipoprotein AI'''|B12='''Gelsolin'''|B13='''Lysozyme'''|B14='''Cystatin C'''|B15='''Fibrinogen Aa-chain'''|B16='''Apolipoprotein AII'''}} | ||
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==References== | ==References== | ||
Revision as of 20:28, 26 November 2019
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Familial amyloidosis Microchapters |
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Diagnosis |
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Treatment |
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Case Studies |
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Familial amyloidosis classification On the Web |
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American Roentgen Ray Society Images of Familial amyloidosis classification |
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Risk calculators and risk factors for Familial amyloidosis classification |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Fahimeh Shojaei, M.D.
Overview
Familiar amyloidosis may be classified according to the type of mutant protein into 7 subtypes: Transthyretin (TTR), apolipoprotein AI, cystatin C, lysozyme, fibrinogen A alpha-chain, gelsolin, and apolipoprotein AII.
Classification
Familiar amyloidosis may be classified according to the type of mutant protein into 7 subtypes:[1][2][3]
- Transthyretin (TTR)
- Apolipoprotein AI
- Apolipoprotein AII
- Fibrinogen Aa
- Lysozyme
- Gelsolin
- Cystatin C
| Genes involved in familial amyloidosis | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Transthyretin (TTR) | Apolipoprotein AI | Gelsolin | Lysozyme | Cystatin C | Fibrinogen Aa-chain | Apolipoprotein AII | |||||||||||||||||||||||||||||||||||||||||||||||||||
| Mutations: • Asp18Glu • Leu55Gln • Asp18Gly • His56Arg • Asp18Asn • Leu58His • Val20Ile • Leu58Arg • Ser23Asn • Thr59Lys • Pro24Ser • Thr60Ala • Ala25Ser • Glu61Lys • Ala25Thr | Mutations: • Gly26Arg • Leu60Arg • Trp50Arg • del60-71 • del70-72 • Leu75Pro • Leu90Pro • Arg173Pro • Leu174Ser • Leu178His | Mutations: • Asp187Asn • Asp187Tyr | Mutations: • Ile56Thr • Asp67His • Trp64Arg • Phe57Ile | Mutation: • Leu68Gln | Mutations: • Arg554Leu • Glu526Val • 4904delG • 4897delT | Mutations: • stop78Gly • stop78Ser • stop78Arg | |||||||||||||||||||||||||||||||||||||||||||||||||||
• Cys10Arg • Leu55Pro • Leu12Pro • Leu55Arg • Phe64Leu • Val28Met • Phe64Ser • Val30Met • Ile68Leu • Val30Ala • Tyr69His • Val30Leu • Tyr69Ile • Val30Gly • Lys70Asn • Phe33Ile • Val71Ala • Phe33Leu • Ile73Val • Phe33Val • Ser77Tyr • Phe33Cys • Ser77Phe • Arg34Thr • Tyr78Phe • Lys35Asn • Ala81Thr • Ala36Pro • Ile84Ser | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
References
- ↑ Benson, Merrill D (2003). "The hereditary amyloidoses". Best Practice & Research Clinical Rheumatology. 17 (6): 909–927. doi:10.1016/j.berh.2003.09.001. ISSN 1521-6942.
- ↑ Benson, Merrill D (2003). "The hereditary amyloidoses". Best Practice & Research Clinical Rheumatology. 17 (6): 909–927. doi:10.1016/j.berh.2003.09.001. ISSN 1521-6942.
- ↑ Scriver, Charles (2001). The metabolic & molecular bases of inherited disease. New York: McGraw-Hill. ISBN 978-0079130358.