
Neuromuscular Home Page
Basic Other · Neuromuscular disease · Dystrophin & Related proteins · Myopathy-related proteins · Muscle proteins: Contractile +... · Mitochondrial pathways · Fatty acid oxidation · Immunotherapy · …
Polyneuropathy Differential Diagnosis
Nov 18, 2025 · Index Search Myopathy Neuropathy Synapse CNS Lab tests Basic Subcellular Washington University ... Go to Differential Diagnosis of Myopathies Return to Neuromuscular Home …
NEUROMUSCULAR PERSONNEL
The Neuromuscular Clinical Laboratory provides Antibody testing Antibodies tested Test request form Neuromuscular pathology (Muscle & Nerve biopsies). We evaluate more than 600 muscle & 100 …
Myopathy Differential Diagnosis
See Neuromuscular Syndromes Go to Differential Diagnosis of Neuropathies Return to Neuromuscular Home Page or newly revised Other revisions 2/14/2024
Motor Syndromes - Washington University in St. Louis
Paraneoplastic Lower Motor Neuron Syndrome 8, 25 Epidemiology: Single patient, 72 year old female Onset: 4 months before diagnosis of tumor Clinical Weakness Asymmetric at onset Arms & Legs …
NEUROMUSCULAR DISEASE: TYPICAL PATTERNS
General: The neuromuscular evaluation Begins with: Evaluation & description of patterns of disease process Gleaned from: History & physical examination Unusual patterns Especially important …
Neuromuscular Clinical Laboratory
Most common preparation Useful for: Inflammatory cells Deficiencies: Fine structure; Myelin pathology; Axon loss Ultrastructure: When necessary Requisition form: Printable PDF Nerve biopsies: …
Additional antibodies include IgM binding to histone H3 and/or GD1a ganglioside and IgG binding to sulfatide and/or GM1 ganglioside. The values of the additional antibody titers are listedon the report. …
MUSCLE BIOPSY - Washington University in St. Louis
GENERAL INDICATIONS FOR MUSCLE BIOPSIES Presence of some evidence of muscle disease Weakness Muscle symptoms: Discomfort; Cramps; Fatigue with activity (r/o myasthenia) Elevated …
Contractures - Washington University in St. Louis
Neuromuscular syndromes: Genotype-Phenotype correlations Missense mutations Onset: Childhood; Mean 2.4 years Weakness: Scapuloperoneal & Facial; Paravertebral weakness or rigidity Tendon …