COEXISTENCE OF TWO CHRONIC NEUROPATHIES IN A YOUNG CHILD: CHARCOT-MARIE-TOOTH DISEASE TYPE 1A AND CHRONIC INFLAMMATORY DEMYELINATING POLYNEUROPATHY

被引:14
|
作者
Marques, Wilson, Jr. [1 ,2 ]
Funayama, Carolina A. R. [1 ]
Secchin, Juliana B. [1 ]
Lourenco, Charles M. [1 ]
Gouvea, Silmara P. [1 ]
Marques, Vanessa D. [1 ]
Bastos, Patricia G. [1 ]
Barreira, Amilton A. [1 ]
机构
[1] Univ Sao Paulo, Sch Med Ribeira Preto, Dept Neurosci & Behav Sci, BR-14049900 Sao Paulo, Brazil
[2] Natl Sci & Technol Inst Translat Med, Sao Paulo, Brazil
关键词
Charcot-Marie-Tooth type 1A; chronic inflammatory demyelinating polyneuropathy; demyelinating neuropathy; hereditary motor and sensory neuropathy type 1A; inflammatory neuropathy; 17P DUPLICATION; HEREDITARY;
D O I
10.1002/mus.21753
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
We report an 18-month-old Charcot-Marie-Tooth type 1A (CMT1A) patient who developed a rapid-onset neuropathy, with proximal and distal weakness, and non-uniform nerve conduction studies. The neuropathy responded well to immunomodulation, confirming the coexistence of an inherited and an inflammatory neuropathy. Unexpected clinical and/ or electrophysiological manifestations in CMT1A patients should alert clinicians to concomitant inflammatory neuropathy. In addition, this association raises reflections about disease mechanism in CMT1A. Muscle Nerve 42: 598-600, 2010
引用
收藏
页码:598 / 600
页数:3
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