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...

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Bibliografiske detaljer
Udgivet i:Case Rep Hematol
Main Authors: Iqbal, Madiha, Jani, Prachi, Ahmed, Salman, Sher, Taimur
Format: Artigo
Sprog:Inglês
Udgivet: Hindawi 2019
Fag:
Case Report
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC6387725/
https://ncbi.nlm.nih.gov/pubmed/30881710
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2019/5092496
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