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Autosomal recessive distal hereditary motor neuropathies
E. Zamba
, K. Christodoulou
, A. K. Al-Qudah
, K. Horani
,
Th Kyriakides
, L. T. Middleton
, A. Mubaidin
Medical School
Cyprus Institute for Neurology and Genetics
Research output
:
Contribution to journal
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Article
›
peer-review
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Keyphrases
Autosomal Recessive
100%
Motor Neuron Disease
100%
Distal Hereditary Motor Neuropathy (dHMN)
100%
Age of Onset
60%
Clinical picture
60%
Autosomal Dominant
40%
Early Disease
20%
Muscle Atrophy
20%
Disability
20%
Rapid Progression
20%
Lower Limb
20%
Motor Function
20%
Novel Form
20%
Mode of Inheritance
20%
Jordan
20%
Jerash
20%
Pyramidal Features
20%
Distal Weakness
20%
Muscle Weakness
20%
Genetic Analysis
20%
Initial Distribution
20%
Cardinal Symptoms
20%
Distal Upper Limb
20%
Upper Limb muscle
20%
X-linked
20%
Muscle Analysis
20%
Heterogeneous Disorder
20%
Benign Course
20%
Type of Inheritance
20%
Sural Nerve
20%
Early Death
20%
Bulbar
20%
Medicine and Dentistry
Disease
100%
Autosomal Recessive Inheritance
100%
Multifocal Motor Neuropathy
100%
Onset Age
50%
Autosomal Dominant Inheritance
33%
Weakness
33%
Infancy
16%
Leg
16%
Upper Limb
16%
Muscle Atrophy
16%
Sural Nerve
16%
Muscle Weakness
16%
Motor Performance
16%
Lower Limb
16%
Genetic Analysis
16%
Biopsy Technique
16%