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ND16590 DNA from Whole Blood

Description:

AMYOTROPHIC LATERAL SCLEROSIS 1; ALS1

Affected:

Yes

Sex:

Female

Age:

54 YR (At Sampling)

  • Overview
  • Characterizations
  • Phenotypic Data
  • External Links

Overview

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Repository NINDS Repository
Subcollection Motor Neuron Disease
Quantity 3 µg
Quantitation Method Please see our FAQ
Biopsy Source Peripheral vein
Sample Source DNA from Whole Blood
Race White
Ethnicity Not Hispanic/Latino
Ethnicity Irish, Italian
Country of Origin USA
Family History Y
Species Homo sapiens
Common Name Human
Note This material represents a finite resource (DNA from Whole Blood)

Characterizations

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Gene SOD1
Chromosomal Location 21q22.11
Allelic Variant 1 147450.0012; AMYOTROPHIC LATERAL SCLEROSIS, FAMILIAL
Identified Mutation ALA4VAL; Deng et al. (1993) found that the ala4-to-val mutation in exon 1 of the SOD1 gene is the most frequent basis for familial amyotrophic lateral sclerosis. This mutation was found in 8 unrelated families. Rosen et al. (1994) confirmed that the ala4-to-val mutation is the most commonly detected of all SOD1 mutations in familial ALS and that it is among the most clinically severe. In comparison with other ALS families, the exon 1 mutation is associated with reduced survival time after onset: 1.2 years, as compared to 2.5 years for all other familial ALS patients.

Phenotypic Data

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Demographic Data
Relation to Proband No Data
Age at Sampling 54 YR
Sex Female
Age of Onset(If not a control) 52 YR
Age at Diagnosis(If not a control) 53 YR
Hispanic or Latino/Not Hispanic or Latino Not Hispanic/Latino
Racial Category White
Country USA
Diagnosed By No Data
 
Data Elements
Clinical Element Type: Motor Neuron Disorders
  (Baseline)
Longitudinal Data
Is this data Longitudinal (Follow-Up) Data? yes  no  
Family History
ALS/other MND present   absent  unknown 
Notes: MOTHER, MATERNAL GREAT AUNT AND UNCLE, M GREAT GRANDMOTHER, MATERNAL COUSIN
Parkinson's disease present   absent  unknown 
Notes: PATERNAL AUNT
Alzheimer's disease present   absent  unknown 
Notes: PATERNAL GRANDMOTHER
Other dementia present  absent   unknown 
Other neurodegenerative disease present  absent   unknown 
Medical History
Alzheimer's disease present  absent  
Ataxia present  absent  
Autism present  absent  
Bipolar (manic-depressive) present  absent  
Brain aneurysm present  absent  
Cancer present   absent 
Dementia Alzheimer's
Dementia
absent
Depression present  absent  
Diabetes present  absent  
Dystonia present  absent  
Epilepsy present  absent  
Heart disease present  absent  
Hypertension present  absent  
Multiple sclerosis present  absent  
Muscle disease present  absent  
Parkinson's present  absent  
Schizophrenia present  absent  
Suicide/Attempt present  absent  
Stroke present  absent  
Primary Clinical Diagnosis
Primary clinical diagnosis  ALS
Notes: HYPERPARATHYROIDISM.
Secondary Neurological Diagnosis
Secondary neurological diagnoses Frontotemporal dementia
Other (specify)
Not Applicable
Site of Symptom Onset
site of symptom onset  Limb-upper
Treatment
Current treatment Riluzole
PEG
NIPPV
Tracheotomy
Assisted Ventilation > 23 hours
Other (specify)
No Treatment

Notes: VIT C, E, SELENIUM, COQ10, VIT D,
Signs Supporting Diagnosis
Upper Motor Neuron Signs-Bulbar definite  indeterminate  absent   not tested 
Upper Motor Neuron Signs-Cervical/upper limbs definite  indeterminate  absent   not tested 
Upper Motor Neuron Signs-Thoracic/chest definite  indeterminate  absent   not tested 
Upper Motor Neuron Signs-Lumbosacral/lower limbs definite  indeterminate  absent   not tested 
Lower Motor Neuron Signs-Bulbar definite  indeterminate   absent  not tested 
Lower Motor Neuron Signs-Cervical/upper limbs definite   indeterminate  absent  not tested 
Lower Motor Neuron Signs-Thoracic/chest definite   indeterminate  absent  not tested 
Lower Motor Neuron Signs-Lumbosacral/lower limbs definite   indeterminate  absent  not tested 
EMG Studies
Bulbar acute denervation  chronic denervation  negative  not examined   acute/chronic denervation 
Cervical/upper limbs acute denervation  chronic denervation  negative  not examined  acute/chronic denervation  
Thoracic/chest acute denervation  chronic denervation  negative  not examined   acute/chronic denervation 
Lumbosacral/lower limbs acute denervation  chronic denervation  negative  not examined  acute/chronic denervation  
Genetics
SOD-1 mutation present   absent  unknown 
Notes: A4V
Other mutation  No Data
Atypical Features of ALS/MND
Atypical features of ALS/MND sensory
autonomic
cerebellar
cognitive
Parkinsonian
sphincter
ocular
other
Optional data
Current ALSFRS-R  No Data
FVC  58% 6/2007
smoking history never   former smoker  current smoker 
years smoking  No Data
Handedness Right  Left   Ambidextrous 

External Links

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NCBI GTR 105400 AMYOTROPHIC LATERAL SCLEROSIS 1; ALS1
OMIM 105400 AMYOTROPHIC LATERAL SCLEROSIS 1; ALS1
Omim Description ALS
  AMYOTROPHIC LATERAL SCLEROSIS
  AMYOTROPHIC LATERAL SCLEROSIS, TYPE 1; ALS1

Culture Protocols

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Supplement -
Pricing
Commercial and Non-U.S.:
$0.00USD
U.S. Academic or
Non-profit:
$0.00USD
NINDS Repository Submitter (past or current) and/or Current NINDS Grantee
$0.00USD
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