دورية أكاديمية

Inflammatory demyelination in a patient with CMT1A.

التفاصيل البيبلوغرافية
العنوان: Inflammatory demyelination in a patient with CMT1A.
المؤلفون: Anne Vital, Claude Vital, Alain Lagueny, Xavier Ferrer, Catherine Ribière-Bachelier, Philippe Latour, Klaus G. Petry
المصدر: Muscle & Nerve; Sep2003, Vol. 28 Issue 3, p373, 4p
مستخلص: We report a case of Charcot-Marie-Tooth disease (CMT), with identified PMP22 gene duplication (CMT type 1A), and with evidence of an inflammatory demyelinating process superimposed on the course of the chronic genetic disease. Macrophage-associated demyelination was observed on the peripheral nerve biopsy. This observation supports some experimental data from the literature and shows that there may be a genetic susceptibility to inflammatory demyelinating processes in certain CMT kindreds. Muscle Nerve 28: 373–376, 2003 [ABSTRACT FROM AUTHOR]
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قاعدة البيانات: Complementary Index
الوصف
تدمد:0148639X
DOI:10.1002/mus.10404