First Report of Hereditary Lysozyme Amyloidosis in a South Asian Family
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...
Saved in:
| Main Authors: | Madiha Iqbal, Prachi Jani, Salman Ahmed, Taimur Sher |
|---|---|
| Format: | Article |
| Language: | English |
| Published: |
Wiley
2019-01-01
|
| Series: | Case Reports in Hematology |
| Online Access: | http://dx.doi.org/10.1155/2019/5092496 |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Cryo-EM structure of a lysozyme-derived amyloid fibril from hereditary amyloidosis
by: Sara Karimi-Farsijani, et al.
Published: (2024-11-01) -
Hereditary transthyretin amyloidosis
by: T. A. Adyan, et al.
Published: (2020-01-01) -
Clinical case of hereditary transthyretin amyloidosis
by: N. Spasova, et al.
Published: (2024-12-01) -
Phenotypic Presentation and Longitudinal Characterization of Hereditary ATTRv Amyloidosis in Previously Undiagnosed Family Members
by: Luca Fazzini, MD, et al.
Published: (2025-08-01) -
A Clinical Case of the Hereditary Transthyretin Amyloidosis
by: E. V. Reznik, et al.
Published: (2021-05-01)