PURPOSE OF REVIEW This article provides an overview of Charcot-Marie-Tooth disease
(CMT) and other inherited neuropathies. These disorders encompass a broad spectrum with …

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Abstract Charcot Marie Tooth (CMT) disease is the most common hereditary sensorimotor
neuropathy that has a slow onset. It presents usually in childhood, starting distally and from …

Charcot-Marie-Tooth (CMT) patients present mainly lower limbs disability, with slowly
progressive distal muscle weakness and atrophy, but hands impairment is a relevant …

Background: Charcot Marie Tooth type 1a (CMT1a) is a primarily demyelinating neuropathy,
characterized by slowly progressive muscle weakness, atrophy, and sensory loss, and is …

Purpose. The aim of the present study was to examine hand function and disability in
persons with Charcot-Marie-Tooth disease (CMT) and to evaluate the possible correlations …

Limited upper limb functioning has impact on restrictions in participation and autonomy of
patients with hereditary motor and sensory neuropathy 1a Page 94 6 Chapter Six Limited …

OBJECTIVE: To assess the prevalence and significance of impaired manual dexterity in
hereditary motor and sensory neuropathy type 1a (HMSN 1a), with the Sollerman hand …

To describe a new test to quantitatively evaluate hand function in patients affected by
Charcot‐Marie‐Tooth neuropathy (CMT). The sensor‐engineered glove test (SEGT) was …

Introdução. A doença de Charcot-Marrie-Tooth (CMT) é uma neuropatia periférica
hereditária caracterizada por atrofia muscular e hipoestesia distal dos membros podendo …