Amyotrophic Lateral Sclerosis 4, Juvenile (ALS4)

Amyotrophic Lateral Sclerosis 4, Juvenile(来自ICD-11)

别称:

Amyotrophic Lateral Sclerosis Type 4

Als4

Distal Hereditary Motor Neuropathy with Upper Motor Neuron Signs

Dhmn with Upper Motor Neuron Signs

Amyotrophic Lateral Sclerosis 4

Neuronopathy, Distal Hereditary Motor, with Pyramidal Features

Neuronopathy Distal Hereditary Motor with Pyramidal Features

Distal Hereditary Motor Neuropathy with Pyramidal Features

Sclerosis, Lateral, Amyotrophic, Type Type 4

Amyotrophic Lateral Sclerosis Juvenile 4

Als 4

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Amyotrophic Lateral Sclerosis 4, Juvenile, also known as amyotrophic lateral sclerosis type 4, is related to frontotemporal dementia and/or amyotrophic lateral sclerosis 4 and oculomotor apraxia, and has symptoms including upper motor neuron signs An important gene associated with Amyotrophic Lateral Sclerosis 4, Juvenile is SETX (Senataxin). Affiliated tissues include spinal cord and brain, and related phenotypes are abnormal pyramidal sign and skeletal muscle atrophy

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