Amyotrophic lateral sclerosis type 4

Orpha code: 357043OMIM code: 602433

Definition

A rare, genetic motor neuron disease characterized by late childhood- or adolescent-onset of slowly progressive, severe, distal limb muscle weakness and wasting, in association with pyramidal signs, normal sensation, and absence of bulbar involvement, leading to degeneration of motor neurons in the brain and spinal cord.

Disease data
Classification

Disease

Synonyms
ALS4
ALS4
dHMN z objawami górnego neuronu ruchowego
Dystalna dziedziczna neuropatia ruchowa z objawami górnego neuronu ruchowego
Distal hereditary motor neuropathy with upper motor neuron signs
dHMN with upper motor neuron signs
ORPHA code
357043
OMIM code
602433
ICD10 code
G12.2
ICD11 code
-

No additional description.

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