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

来源：

MUSCLE & NERVE | 2010年 / 42卷 / 04期

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

页码：598 / 600

页数：3

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