Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 1 (ALS-PDC1)

Alias:
Guam Disease
Lytico-Bodig Disease
Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex of Guam
Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 1, Susceptibility to
Amyotrophic Lateral Sclerosis-Parkinsonism-Dementia Complex
Parkinson-Dementia Complex of Guam
Guam Parkinsonism-Dementia Complex
Als-Pdc
G-Pdc
Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex, Susceptibility to
Amyotrophic Lateral Sclerosis-Parkinsonism-Dementia of Guam Syndrome
Sclerosis, Lateral, Amyotrophic/parkinsonism/dementia Complex 1
Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex
Amyotrophic Lateral Sclerosis, Guam Form
Parkinsonism-Dementia-Als Complex
Amyotrophic Lateral Sclerosis
Parkinsonian Disorders
Als/pdc of Guam
Als-Pdc1
Pdals
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 1, also known as guam disease, is related to frontotemporal dementia and/or amyotrophic lateral sclerosis 4 and amyotrophic lateral sclerosis 19, and has symptoms including tremor, bradykinesia and abnormality of extrapyramidal motor function. An important gene associated with Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 1 is TRPM7 (Transient Receptor Potential Cation Channel Subfamily M Member 7), and among its related pathways/superpathways are Neuroscience and Copper homeostasis. The drugs Olanzapine and Risperidone have been mentioned in the context of this disorder. Affiliated tissues include bone marrow and spinal cord, and related phenotypes are cerebral atrophy and dementia
Related ID:

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AD
Unknown
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19
264
23

Medical Symptom

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Description
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Gene & Mutation

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Disease Model

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MGI
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Publications
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References Literature

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