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Finger Flexion Weakness

Muscular Dystrophy

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Overview

From WUSTL Neuromuscular

Common: Selective & Severe Inclusion-Body Myositis (IM-VAMP) Myotonic Dystrophy 1 Other Acquired Sarcoid Hereditary Myotonic Dystrophy 2 Dystrophy: Dystrophin; Dysferlin; LAMA2 Storage: αB-Crystallin; Filamin; MYH7; VCP Metabolic: Pompe (Acid Maltase); GNE Contractures: HNRNPDL

Related Conditions

Shared genes

Asymmetric Myopathic Weakness

Granulomatous Myopathies

Immune & Inflammatory Myopathies: Neoplasm Associations

Inclusion Body Myositis (IBM)

Inflammatory & Immune Myopathies (IIM): Acquired

RNAVAMPINCLUSION

Inflammatory Myopathy + Mitochondrial Pathology in muscle (IM-Mito), subtype of IM-VAMP

Muscle Fiber Pathology

Other Muscle Features

VAMPINCLUSIONBCIM

External Resources

WUSTL Neuromuscular

Washington University Disease Center

Biomedical Literature

NCBI Expert-Authored Reviews

Portal for Rare Diseases

National Organization for Rare Disorders

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