Neuromuscular HOMEepAGE
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Asymmetric Myopathic Weakness

De NovoMuscular Dystrophy
W
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Overview

From WUSTL Neuromuscular

Hereditary myopathies Facioscapulohumeral Dystrophy McLeod Syndrome Glycogen storage disorders: Some patients Phosphorylase deficiency (McArdle's) Acid maltase deficiency (Adult onset) Neutral lipid storage disease Distal myopathy Atypical Miyoshi: Dysferlin Vocal cord & Pharyngeal: Matrin 3 MPD3 MPD4: Filamin C MSP4: SQSTM1 LGD 1C: Caveolin-3 2A: Calpain-3 2B (Miyoshi myopathy): Dysferlin 2I: FKRP 2L: Anoctamin 5 Dystrophinopathy: Female carriers Other myopathies Reducing body myopathy: FHL1 IBMPFD: VCP ACTA1 rod myopathy: Mosaic (de novo) mutation Carriers, Manifesting female Dystrophinopath

Related Conditions

Shared genes
Finger Flexion Weakness
VAMP
Granulomatous Myopathies
VAMP
Immune & Inflammatory Myopathies: Neoplasm Associations
VPVAMP
Inclusion Body Myositis (IBM)
VAMPIADRB1
Inflammatory & Immune Myopathies (IIM): Acquired
RNAVAMPINCLUSION
Inflammatory Myopathy + Mitochondrial Pathology in muscle (IM-Mito), subtype of IM-VAMP
VAMP
Muscle Fiber Pathology
VPSRPVAMP
Other Muscle Features
VAMPINCLUSIONBCIM

External Resources

WUSTL Neuromuscular
Washington University Disease Center
PubMed
Biomedical Literature
GeneReviews
NCBI Expert-Authored Reviews
Orphanet
Portal for Rare Diseases
NORD
National Organization for Rare Disorders

Data sourced from the Washington University Neuromuscular Disease Center. For clinical use, always refer to primary sources.