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GM23742 LCL from B-Lymphocyte

Description:

AMYOTROPHIC LATERAL SCLEROSIS 1; ALS1

Affected:

Yes

Sex:

Male

Age:

56 YR (At Sampling)

  • Overview
  • Characterizations
  • Phenotypic Data
  • External Links
  • Culture Protocols

Overview

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Repository NIGMS Human Genetic Cell Repository
Subcollection Heritable Diseases
Biopsy Source Peripheral vein
Cell Type B-Lymphocyte
Tissue Type Blood
Transformant Epstein-Barr Virus
Sample Source LCL from B-Lymphocyte
Race More than one race
Ethnicity AMERICAN INDIAN/CAUCASIAN
Country of Origin USA
Family History N
Relation to Proband proband
Confirmation Clinical summary/Case history
Species Homo sapiens
Common Name Human
Remarks Clinically affected; onset of symptoms at age 54 years; difficulty swallowing; dysphonia; atrophy/weakness of tongue and facial muscles; fasciculations involving the extremities; bilateral brisk reflexes; absence of any sensory findings; shortness of breath; EMG nerve conduction studies revealed: reduced sensory nerve action potential amplitudes of bilateral median nerves with prolonged latencies, markedly prolonged distal motor latencies of bilateral median nerves with reduced to borderline normal CMAP amplitudes; conduction velocity proximally is borderline normal to slightly slowed, absent right median and ulnar F-responses while right posterior tibial F-response latency is significantly prolonged, left median F response latency is very much prolonged; needle electromyography results revealed fasciculation potentials in the majority of muscles sampled, increased proportion of high amplitude, long duration, polyphasic units with reduced recruitment pattern, APB muscles reveal disproportionately more denervation; possible coexisting neuropathy, polyradiculopathy in addition to ALS considered due to presence of abnormal sensory nerve conduction velocities and more severely reduced velocities and conduction velocities; subject uses communication/learning device and speech, occupational and physical therapy; positive family history: mother, aunt and first cousin were also affected (not in repository).

Characterizations

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IDENTIFICATION OF SPECIES OF ORIGIN Species of Origin Confirmed by LINE assay
 

Phenotypic Data

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Remarks Clinically affected; onset of symptoms at age 54 years; difficulty swallowing; dysphonia; atrophy/weakness of tongue and facial muscles; fasciculations involving the extremities; bilateral brisk reflexes; absence of any sensory findings; shortness of breath; EMG nerve conduction studies revealed: reduced sensory nerve action potential amplitudes of bilateral median nerves with prolonged latencies, markedly prolonged distal motor latencies of bilateral median nerves with reduced to borderline normal CMAP amplitudes; conduction velocity proximally is borderline normal to slightly slowed, absent right median and ulnar F-responses while right posterior tibial F-response latency is significantly prolonged, left median F response latency is very much prolonged; needle electromyography results revealed fasciculation potentials in the majority of muscles sampled, increased proportion of high amplitude, long duration, polyphasic units with reduced recruitment pattern, APB muscles reveal disproportionately more denervation; possible coexisting neuropathy, polyradiculopathy in addition to ALS considered due to presence of abnormal sensory nerve conduction velocities and more severely reduced velocities and conduction velocities; subject uses communication/learning device and speech, occupational and physical therapy; positive family history: mother, aunt and first cousin were also affected (not in repository).

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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Split Ratio 1:3
Temperature 37 C
Percent CO2 5%
Percent O2 AMBIENT
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
International/Commercial/For-profit:
$373.00USD
U.S. Academic/Non-profit/Government:
$216.00USD
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