Atypical Presentation of Gelsolin Amyloidosis in a Man of African Descent with a Novel Mutation in the Gelsolin Gene

Patient: Male, 60 Final Diagnosis: Atypical gelsolin amyloidosis Symptoms: Cranial nerve palsy • proximal muscle weakness Medication: — Clinical Procedure: — Specialty: Hematology OBJECTIVE: Rare disease BACKGROUND: Gelsolin amyloidosis is a very rare systemic disease presenting with a pathognomonic...

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Detalles Bibliográficos
Autores principales: Oregel, Karlos Z., Shouse, Geoffrey P., Oster, Cyrus, Martinez, Freddy, Wang, Jun, Rosenzweig, Michael, Deisch, Jeremy K., Chen, Chien-Shing, Nagaraj, Gayathri
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Scientific Literature, Inc. 2018
Materias:
Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5890616/
https://www.ncbi.nlm.nih.gov/pubmed/29599423
http://dx.doi.org/10.12659/AJCR.907550

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5890616/
https://www.ncbi.nlm.nih.gov/pubmed/29599423
http://dx.doi.org/10.12659/AJCR.907550

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