Severe axonal neuropathy resultıng from folıc acıd defıcıency ın a case wıth restrıctıve type anorexıa nervosa
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Case report
VOLUME: 4 ISSUE: 1
P: 72 - 74
2014

Severe axonal neuropathy resultıng from folıc acıd defıcıency ın a case wıth restrıctıve type anorexıa nervosa

J Dr Behcet Uz Child Hosp 2014;4(1):72-74
1. Dokuz Eylul University Hospital, Division Of Pediatric Neurology, Izmir, Turkey
2. Dokuz Eylul University Hospital, Department Of Neurology, Izmir, Turkey
3. Dokuz Eylul University, Institute Of Health Sciences, Izmir, Turkey
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Received Date: 2013-06-04T23:02:03
Accepted Date: 2014-04-11T12:16:10
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Abstract

An adolescent patient with eating disorder and three months history of severe weight loss presented with signs of neuropathy. She had severe symmetrical weakness of proximal and distal muscles and electromyography revealed axonal type sensorimotor neuropathy. Serum folic acid level was low (1.5 ng/ml; normal values 5-16 ng/ml). Although peripheral neuropathy is a rare late complication of anorexia nervosa, clinicians dealing with anorexia nervosa should be aware that peripheral neuropathy may also develop in the early course of disease.

Keywords:
Anorexia nervosa, sensorimotor neuropathy, electromyography, children