Familial polyneuropathy with anti-myelin-associated glycoprotein antibodies
Autor: | Elijah W. Stommel, D. Yang, V. G. Tseng, Brent T. Harris, H. R. Jones, Jayashri Srinivasan |
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Rok vydání: | 2005 |
Předmět: |
Gait Ataxia
Male medicine.medical_specialty Pathology Weakness Polyradiculoneuropathy Chronic inflammatory demyelinating polyneuropathy Hypesthesia Antibodies Monoclonal Murine-Derived Disability Evaluation Polyneuropathies Myelin Internal medicine medicine Humans Immunologic Factors Peripheral Nerves Myelin Sheath Aged Autoantibodies Leg biology Proprioception Myelin-associated glycoprotein business.industry Siblings Antibodies Monoclonal Recovery of Function medicine.disease Myelin-Associated Glycoprotein Treatment Outcome medicine.anatomical_structure Endocrinology Immunoglobulin M Monoclonal biology.protein Neurology (clinical) medicine.symptom Rituximab business Polyneuropathy |
Zdroj: | Neurology. 64:1983-1984 |
ISSN: | 1526-632X 0028-3878 |
DOI: | 10.1212/01.wnl.0000163994.27792.18 |
Popis: | We describe the occurrence of the anti-myelin-associated glycoprotein (anti-MAG) syndrome, a well-recognized variant of chronic inflammatory demyelinating polyneuropathy (CIDP) with distinct clinical and electrophysiologic characteristics, in two brothers. A 70-year-old man presented with symmetric numbness distal to his knees, followed by progressive imbalance and gait unsteadiness that developed over 2 years. His similarly affected brother is described below (Case 2); there was no other relevant family history. On examination he had mild distal weakness in both lower limbs and symmetric vibration and proprioceptive loss distally in all four limbs. Muscle stretch reflexes were absent. Gait was severely ataxic and Romberg's sign was present. Nerve conduction studies revealed a severe demyelinating polyneuropathy with disproportionate distal slowing, prolongation of F waves without evidence of conduction block, and met criteria for CIDP.1 Immunoglobulin M (IgM) kappa monoclonal gammopathy was identified; IgM was 235 mg/dL (normal, 50 to 200 mg/dL) of which 50% to 90% was monoclonal and anti-MAG reactivity was positive at a titer of … |
Databáze: | OpenAIRE |
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