Hereditary lysozyme amyloidosis with sicca syndrome, digestive, arterial, and tracheobronchial involvement: case-based review-Reference-Cited by-同舟云学术

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Hereditary lysozyme amyloidosis with sicca syndrome, digestive, arterial, and tracheobronchial involvement: case-based review

Published:2017-09-30 Issue:11 Volume:36 Page:2623-2628
ISSN:0770-3198
Container-title:Clinical Rheumatology
language:en
Short-container-title:Clin Rheumatol

Author:

Benyamine Audrey,Bernard-Guervilly Fanny,Tummino Céline,Macagno Nicolas,Daniel Laurent,Valleix Sophie,Granel Brigitte

Publisher

Springer Science and Business Media LLC

Subject

General Medicine,Rheumatology

Link

http://link.springer.com/article/10.1007/s10067-017-3839-7/fulltext.html

Reference19 articles.

1. Pepys MB, Hawkins PN, Booth DR, Vigushin DM, Tennent GA, Soutar AK et al (1993) Human lysozyme gene mutations cause hereditary systemic amyloidosis. Nature 362:553–557. https://doi.org/10.1038/362553a0

2. Lanham JG, Meltzer ML, de Beer FC, Hughes GRV, Pepys MB (1982) Familial amyloidosis of Ostertag. Q J Med 51:25–32

3. Gillmore JD, Booth DR, Madhoo S, Pepys MB, Hawkins PN (1999) Hereditary renal amyloidosis associated with variant lysozyme in a large English family. Nephrol Dial Transplant 14:2639–2644

4. Harrison RF, Hawkins PN, Roche WR, MacMahon RFT, Hubscher SG, Buckels JA (1996) “Fragile” liver and massive hepatic haemorrhage due to hereditary amyloidosis. Gut 38:151–152

5. Mells GFG, Buckels JA, Thorburn D (2006) Emergency liver transplantation for hereditary lysozyme amyloidosis. Liver Transpl 12:1908–1909. https://doi.org/10.1002/lt.20984

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3. Nonneoplastic pathology of the large and small airways;Practical Pulmonary Pathology;2024

4. Management of tracheobronchial amyloidosis: a review of the literature;ERJ Open Research;2023-11-09

5. First Report of Lysozyme Amyloidosis with p.F21L/T88N Amino Acid Substitutions in a Russian Family;International Journal of Molecular Sciences;2023-09-22

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