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

摘要

>Patient: Male, 60>Final Diagnosis: Atypical gelsolin amyloidosis>Symptoms: Cranial nerve palsy • proximal muscle weakness>Medication: —>Clinical Procedure: —>Specialty: HematologyObjective:>Rare disease