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search submit
ND12205
DNA
from
LCL
Description:
AMYOTROPHIC LATERAL SCLEROSIS 1; ALS1
ALS PANEL; BULBAR ONSET; ALL DEFINITE ALS
Affected:
Yes
Gender:
Female
Age:
68
YR
(At Sampling)
Sample Description
Overview
Phenotypic Data
Publications
External Links
Overview
Repository
NINDS Repository
Subcollection
Motor Neuron Disease
Quantity
3 µg
Quantitation Method
Please see our
FAQ
Biopsy Source
Peripheral vein
Cell Type
B-Lymphocyte
Tissue Type
Blood
Transformant
Epstein-Barr Virus
Sample Source
DNA from LCL
Race
White
Ethnicity
Not Hispanic/Latino
Country of Origin
USA
Family History
Y
Species
Homo
sapiens
Common Name
Human
Phenotypic Data
Demographic Data
Relation to Proband
No Data
Age at Sampling
68 YR
Gender
Female
Age of Onset(If not a control)
66 YR
Age at Diagnosis(If not a control)
67 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
Parkinson's disease
present
absent
unknown
Notes:
FATHER
Alzheimer's disease
present
absent
unknown
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
Secondary Neurological Diagnosis
Secondary neurological diagnoses
Frontotemporal dementia
Other (specify)
Not Applicable
Site of Symptom Onset
site of symptom onset
Bulbar
Treatment
Current treatment
Riluzole
PEG
NIPPV
Tracheotomy
Assisted Ventilation > 23 hours
Other (specify)
No Treatment
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
No Data
Notes:
NOT TESTED
Other mutation
No Data
Notes:
NOT TESTED
Atypical Features of ALS/MND
Atypical features of ALS/MND
sensory
autonomic
cerebellar
cognitive
Parkinsonian
sphincter
ocular
other
Optional data
Current ALSFRS-R
23/48
FVC
36%
smoking history
never
former smoker
current smoker
years smoking
4 YRS.
Handedness
Right
Left
Ambidextrous
Publications
Abramzon Y, Johnson JO, Scholz SW, Taylor JP, Brunetti M, Calvo A, Mandrioli J, Benatar M, Mora G, Restagno G, Chiò A, Traynor BJ
, Valosin-containing protein (VCP) mutations in sporadic amyotrophic lateral sclerosis Neurobiology of aging33:2231.e1-6 2012
PubMed ID:
22572540
External Links
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
dbGaP Link
phs000101.v5.p1
Culture Protocols
Temperature
37 C
Percent CO2
5%
Medium
Roswell Park Memorial Institute Medium 1640 with 2mM L-glutamine or equivalent
Serum
15% fetal bovine serum Not Inactivated
Substrate
None specified
Subcultivation Method
dilution - add fresh medium
Supplement
-
Pricing
Commercial and Non-U.S.:
$0.00
USD
U.S. Academic or
Non-profit:
$0.00
USD
NINDS Repository Submitter (past or current) and/or Current NINDS Grantee
$0.00
USD
Add to Cart
How to Order
Ordering Instructions
MTA / Assurance Form
Statement of Research Intent Form
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