Myofibrillar myopathy presenting with an inclusion body myositis-like phenotype

Muscle Nerve. 2023 May;67(5):E15-E17. doi: 10.1002/mus.27806. Epub 2023 Mar 7.

Authors

Frank Diaz^{1

2}, Payam Soltanzadeh³, Shaweta Khosa^{2

3}, Negar Khanlou⁴, Robert Freundlich², Shri K Mishra^{2

3

5}

Affiliations

¹ Department of Neurology, Cedars-Sinai Medical Center, Los Angeles, California, USA.
² Department of Neurology, Olive View-UCLA Medical Center, Sylmar, California, USA.
³ Department of Neurology, David Geffen School of Medicine at UCLA, Los Angeles, California, USA.
⁴ Department of Pathology, David Geffen School of Medicine at UCLA, Los Angeles, California, USA.
⁵ Department of Neurology, Keck School of Medicine, Los Angeles, California, USA.

PMID: 36815757
DOI: 10.1002/mus.27806

No abstract available

Keywords: LDB3; ZASPopathies; distal myopathy; inclusion body myositis; myofibrillar myopathy.

Publication types

Letter

MeSH terms

Humans
Muscle, Skeletal
Myopathies, Structural, Congenital* / diagnosis
Myopathies, Structural, Congenital* / genetics
Myositis*
Myositis, Inclusion Body* / complications
Myositis, Inclusion Body* / diagnosis
Myositis, Inclusion Body* / genetics
Phenotype

Supplementary concepts

Myofibrillar Myopathy