First Report of Hereditary Lysozyme Amyloidosis in a South Asian Family
First Report of Hereditary Lysozyme Amyloidosis in a South Asian Family
About this item
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Author / Creator
Publisher
Cairo, Egypt: Hindawi Publishing Corporation
Journal title
Language
English
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Publication information
Publisher
Cairo, Egypt: Hindawi Publishing Corporation
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Scope and Contents
Contents
Lysozyme amyloidosis (ALys) is an exceedingly rare autosomal dominant hereditary type of systemic amyloidosis that can be misdiagnosed as other common types of systemic amyloidosis. The gastrointestinal tract and the kidney are the most common sites of organ involvement. No specific treatment exists for ALys, and the management primarily consists o...
Alternative Titles
Full title
First Report of Hereditary Lysozyme Amyloidosis in a South Asian Family
Authors, Artists and Contributors
Author / Creator
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Record Identifier
TN_cdi_doaj_primary_oai_doaj_org_article_826681184d6d44c5ac0d87be0f5fc949
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_826681184d6d44c5ac0d87be0f5fc949
Other Identifiers
ISSN
2090-6560
E-ISSN
2090-6579
DOI
10.1155/2019/5092496
