The case reminds clinicians to include ZASP MFM in their differential diagnosis of distal late-onset myopathies and that a genetic blood test is.
Early adult onset distal myopathy Type 3 (Laing). Centronuclear myopathy. Debrancher deficiency. Hereditary Inclusion Body Myopathy. Inclusion Body Myositis.
Sporadic late-onset nemaline myopathy (SLONM) is a rare, late-onset muscle disorder, characterized by the presence of nemaline rods in muscle fibers. Sporadic late-onset nemaline myopathy (SLONM) is a rare, acquired, late-onset muscle disorder with subacute progression.
AANEM 57th Annual Meeting. Québec City, Québec, Canada. Adult Onset Myopathies. American Association of Neuromuscular & Electrodiagnostic Medicine e.