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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Detalles Bibliográficos
Autores principales: Iqbal, Madiha, Jani, Prachi, Ahmed, Salman, Sher, Taimur
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2019
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6387725/
https://www.ncbi.nlm.nih.gov/pubmed/30881710
http://dx.doi.org/10.1155/2019/5092496

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6387725/
https://www.ncbi.nlm.nih.gov/pubmed/30881710
http://dx.doi.org/10.1155/2019/5092496

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