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Med J Tabriz Uni Med Sciences Health Services. 2004;26(3): 99-103.
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Research

Two Cases of Isaac’s Syndrome Associated with Charcot – Marie – Tooth Neuropathy as a Hereditary Disorder

OSHIB NATTAJ A, RAHBAR M
*Corresponding Author:

Abstract

A 21-year-old man and a 16-year-old girl (sibling) developed generalized relatively slow , undulating and worm - like movements of the muscles (myokymia), cramps and stiffness since childhood. Myokymia was continued during sleep. Symptoms exacerbated with unoptimal temprature of enviroment (cold , warm), physical activity and sleep awakening at morning. They had excessive sweating and limited physical activity. The male patient developed a diffuse subcutaneous nodules and symmetric muscular hypertrophy (quadriceps and calf) and carpopedal spasm. There was ankle joint contracture, without significant sensory and motor abnormalities, absent ankle reflex and reduced other deep tendon reflexes, high arch feet and normal laboratory tests. Nerve conduction study showed low amplitude and slowing of sensory and motor responses, F waves and H-reflexes with repetitive-after-discharge, especially in lower limbs and normal repetitive stimulation test. Electromyography displayed a significant spontaneous activity including myokymic, neuromyotonic, doublet, triplet discharges with neurogenic motor unite action potentials. Significant improvement was seen with carbmazepine.
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Submitted: 28 Jul 2013
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