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Amyloid Neuropathies, Familial

"Amyloid Neuropathies, Familial" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus, MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure, which enables searching at various levels of specificity.

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Inherited disorders of the peripheral nervous system associated with the deposition of AMYLOID in nerve tissue. The different clinical types based on symptoms correspond to the presence of a variety of mutations in several different proteins including transthyretin (PREALBUMIN); APOLIPOPROTEIN A-I; and GELSOLIN.

Descriptor ID	D028227
MeSH Number(s)	C10.574.500.050 C10.668.829.050.050 C16.320.400.050 C16.320.565.176.050 C18.452.648.176.050 C18.452.845.500.050.050 C18.452.845.500.075.050
Concept/Terms	Amyloid Neuropathies, Familial Amyloid Neuropathies, Familial Amyloid Neuropathy, Familial Familial Amyloid Neuropathies Familial Amyloid Neuropathy Neuropathies, Familial Amyloid Neuropathy, Familial Amyloid Hereditary Neuropathic Amyloidosis Amyloidoses, Hereditary Neuropathic Amyloidosis, Hereditary Neuropathic Hereditary Neuropathic Amyloidoses Neuropathic Amyloidoses, Hereditary Neuropathic Amyloidosis, Hereditary Familial Amyloid Polyneuropathies Amyloid Polyneuropathies, Familial Amyloid Polyneuropathy, Familial Familial Amyloid Polyneuropathy Polyneuropathies, Familial Amyloid Polyneuropathy, Familial Amyloid Familial Amyloid Polyneuropathy, Type VI Familial Amyloid Polyneuropathy, Type VI Type VI Familial Amyloid Polyneuropathy Amyloid Polyneuropathy, British Type Amyloid Polyneuropathy, British Type Type III Familial Amyloid Polyneuropathy Familial Amyloid Polyneuropathy, Type III Iowa Type Amyloid Polyneuropathy Amyloid Polyneuropathy, Iowa Type British Type Amyloid Polyneuropathy Familial Amyloid Polyneuropathy, Type IV Familial Amyloid Polyneuropathy, Type IV Type IV Familial Amyloid Polyneuropathy Familial Amyloid Neuropathy, Portuguese Type Familial Amyloid Neuropathy, Portuguese Type Familial Amyloid Neuropathy, Andrade Type Familial Amyloid Polyneuropathy, Type I Familial Portuguese Polyneuritic Amyloidosis Wohlwill-Corino Andrade Syndrome Syndrome, Wohlwill-Corino Andrade Wohlwill Corino Andrade Syndrome Polyneuritic Amyloidosis, Portuguese Amyloidoses, Portuguese Polyneuritic Amyloidosis, Portuguese Polyneuritic Polyneuritic Amyloidoses, Portuguese Portuguese Polyneuritic Amyloidoses Portuguese Polyneuritic Amyloidosis Portuguese Type Familial Amyloid Neuropathy Type I Familial Amyloid Polyneuropathy Wohlwill-Andrade Syndrome Syndrome, Wohlwill-Andrade Wohlwill Andrade Syndrome Amyloid Neuropathy Type 1 Neuropathic Amyloid Syndrome Amyloid Syndrome, Neuropathic Amyloid Syndromes, Neuropathic Neuropathic Amyloid Syndromes Syndrome, Neuropathic Amyloid Syndromes, Neuropathic Amyloid Familial Amyloid Polyneuropathy, Appalachian Type Familial Amyloid Polyneuropathy, Appalachian Type Appalachian Type Familial Amyloid Polyneuropathy Familial Amyloid Polyneuropathy, Jewish Type Familial Amyloid Polyneuropathy, Jewish Type Jewish Type Familial Amyloid Polyneuropathy Familial Amyloid Polyneuropathy, Type V Familial Amyloid Polyneuropathy, Type V Finnish Type Familial Amyloid Neuropathy Type V Familial Amyloid Polyneuropathy Familial Amyloid Neuropathy, Finnish Type Amyloid Polyneuropathy, Swiss Type Amyloid Polyneuropathy, Swiss Type Swiss Type Amyloid Polyneuropathy Type II Familial Amyloid Polyneuropathy Familial Amyloid Polyneuropathy, Type II

Below are MeSH descriptors whose meaning is more general than "Amyloid Neuropathies, Familial".

Diseases [C]
Nervous System Diseases [C10]
Neurodegenerative Diseases [C10.574]
Heredodegenerative Disorders, Nervous System [C10.574.500]
Amyloid Neuropathies, Familial [C10.574.500.050]
Neuromuscular Diseases [C10.668]
Peripheral Nervous System Diseases [C10.668.829]
Amyloid Neuropathies [C10.668.829.050]
Amyloid Neuropathies, Familial [C10.668.829.050.050]
Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
Genetic Diseases, Inborn [C16.320]
Heredodegenerative Disorders, Nervous System [C16.320.400]
Amyloid Neuropathies, Familial [C16.320.400.050]
Metabolism, Inborn Errors [C16.320.565]
Amyloidosis, Familial [C16.320.565.176]
Amyloid Neuropathies, Familial [C16.320.565.176.050]
Nutritional and Metabolic Diseases [C18]
Metabolic Diseases [C18.452]
Metabolism, Inborn Errors [C18.452.648]
Amyloidosis, Familial [C18.452.648.176]
Amyloid Neuropathies, Familial [C18.452.648.176.050]
Proteostasis Deficiencies [C18.452.845]
Amyloidosis [C18.452.845.500]
Amyloid Neuropathies [C18.452.845.500.050]
Amyloid Neuropathies, Familial [C18.452.845.500.050.050]
Amyloidosis, Familial [C18.452.845.500.075]
Amyloid Neuropathies, Familial [C18.452.845.500.075.050]

Below are MeSH descriptors whose meaning is related to "Amyloid Neuropathies, Familial".

Below are MeSH descriptors whose meaning is more specific than "Amyloid Neuropathies, Familial".

Publications

Timeline | Most Recent

This graph shows the total number of publications written about "Amyloid Neuropathies, Familial" by people in this website by year, and whether "Amyloid Neuropathies, Familial" was a major or minor topic of these publications.

Bar chart showing 33 publications over 4 distinct years, with a maximum of 13 publications in 2017

To see the data from this visualization as text, click here.

Year	Major Topic	Minor Topic	Total
2017	12	1	13
2018	10	2	12
2019	6	1	7
2021	1	0	1

Below are the most recent publications written about "Amyloid Neuropathies, Familial" by people in Profiles.

Expert consensus on the monitoring of transthyretin amyloid cardiomyopathy. Eur J Heart Fail. 2021 06; 23(6):895-905.

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ATTR amyloidosis during the COVID-19 pandemic: insights from a global medical roundtable. Orphanet J Rare Dis. 2021 05 06; 16(1):204.

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Treatment of cardiac transthyretin amyloidosis: an update. Eur Heart J. 2019 12 01; 40(45):3699-3706.

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Association between hearing loss and hereditary ATTR amyloidosis. Amyloid. 2019 Dec; 26(4):234-242.

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Expert Consensus Recommendations for the Suspicion and Diagnosis of Transthyretin Cardiac Amyloidosis. Circ Heart Fail. 2019 09; 12(9):e006075.

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Pharyngo-laryngeal involvement in systemic amyloidosis with cardiac involvement: a prospective observational study. Amyloid. 2019 Dec; 26(4):216-224.

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Screening for Transthyretin Amyloid Cardiomyopathy in Everyday Practice. JACC Heart Fail. 2019 08; 7(8):709-716.

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Effects of Patisiran, an RNA Interference Therapeutic, on Cardiac Parameters in Patients With Hereditary Transthyretin-Mediated Amyloidosis. Circulation. 2019 01 22; 139(4):431-443.

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Tafamidis for Transthyretin Amyloid Cardiomyopathy. N Engl J Med. 2019 01 10; 380(2):196-197.

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[The Changing Appearance of Cardiac Amyloidosis]. Dtsch Med Wochenschr. 2018 09; 143(18):1335-1343.

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Amyloid Neuropathies, Familial