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GM24729 LCL from B-Lymphocyte

Description:

INCLUSION BODY MYOPATHY 2, AUTOSOMAL RECESSIVE; IBM2

Affected:

Yes

Sex:

Female

Age:

53 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
Muscular Dystrophies
CMD Specific
PIGI Consented Sample
Biopsy Source Peripheral vein
Cell Type B-Lymphocyte
Tissue Type Blood
Transformant Epstein-Barr Virus
Sample Source LCL from B-Lymphocyte
Race White
Ethnicity Not Hispanic/Latino
Ethnicity ENGLISH/GERMAN
Country of Origin USA
Family History Y
Relation to Proband proband
Confirmation Biochemical characterization before cell line submission to CCR
Species Homo sapiens
Common Name Human
Remarks Clinically affected; progressive muscle weakness, proximal greater than distal; increasing weakness of upper and lower extremities; normal copy number of SMN1 and SMN2; whole blood genomic DNA sequencing of GNE coding region did not reveal any pathogenic variants; surgical neuropathology report for left quadriceps skeletal muscle biopsy at 47 years of age revealed primary myopathy with changes suggestive of hereditary inclusion body myopathy - rimmed vacuoles, fibers undergoing degeneration; absence of inflammatory infiltrate exclude possibility of inclusion body myositis and suggest the hereditary form of disease; morphology and histochemistry suggest mild denervation; H&E staining revealed variation the diameter of the muscle fibers with the large majority within a relatively narrow range (40-75 micrometers) and some markedly atrophic fibers - some with angulated profiles on cross sections and a few extremely atrophic appearing as small "nuclear bags"; other cytologic abnormalities include myofiber necrosis, phagocytosis, inclusion bodies, basophilic fibers with regeneration and other unidentified abnormalities; no significant fibrosis in the endomysium and perimysium; no inflammatory infiltrates, vasculitis, or granulomas; PAS and oil red O staining reveal normal amounts of glycogen and neutral lipids; histochemical staining for activity of ATPase and NADH revealed normal demarcation between type 1 and type 2 fibers; dark atrophic fibers were seen in sections stained for NADH activity, sometimes with angulated profiles on cross sections; immunoperoxidase stainings for sarcoglycans (alpha, delta, and beta), merosin, emerin, desmin, dystroglycan, myotillin, dysferlin, and spectrin show a normal membranous reaction pattern; Chron's disease; problems with a lumbar disc resulted in ordering of orthotics; family history for neuromuscular disease in: father, brother, paternal uncle and aunt, paternal grandmother, two paternal male cousins; two unaffected paternal cousins, unaffected fraternal twin; medications: Lamictal XR, Fluoxetine, Trazodone, Diovan HCT, Fish oil, Cyanocobalm

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; progressive muscle weakness, proximal greater than distal; increasing weakness of upper and lower extremities; normal copy number of SMN1 and SMN2; whole blood genomic DNA sequencing of GNE coding region did not reveal any pathogenic variants; surgical neuropathology report for left quadriceps skeletal muscle biopsy at 47 years of age revealed primary myopathy with changes suggestive of hereditary inclusion body myopathy - rimmed vacuoles, fibers undergoing degeneration; absence of inflammatory infiltrate exclude possibility of inclusion body myositis and suggest the hereditary form of disease; morphology and histochemistry suggest mild denervation; H&E staining revealed variation the diameter of the muscle fibers with the large majority within a relatively narrow range (40-75 micrometers) and some markedly atrophic fibers - some with angulated profiles on cross sections and a few extremely atrophic appearing as small "nuclear bags"; other cytologic abnormalities include myofiber necrosis, phagocytosis, inclusion bodies, basophilic fibers with regeneration and other unidentified abnormalities; no significant fibrosis in the endomysium and perimysium; no inflammatory infiltrates, vasculitis, or granulomas; PAS and oil red O staining reveal normal amounts of glycogen and neutral lipids; histochemical staining for activity of ATPase and NADH revealed normal demarcation between type 1 and type 2 fibers; dark atrophic fibers were seen in sections stained for NADH activity, sometimes with angulated profiles on cross sections; immunoperoxidase stainings for sarcoglycans (alpha, delta, and beta), merosin, emerin, desmin, dystroglycan, myotillin, dysferlin, and spectrin show a normal membranous reaction pattern; Chron's disease; problems with a lumbar disc resulted in ordering of orthotics; family history for neuromuscular disease in: father, brother, paternal uncle and aunt, paternal grandmother, two paternal male cousins; two unaffected paternal cousins, unaffected fraternal twin; medications: Lamictal XR, Fluoxetine, Trazodone, Diovan HCT, Fish oil, Cyanocobalm

External Links

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NCBI GTR 605820 NONAKA MYOPATHY; NM
OMIM 605820 NONAKA MYOPATHY; NM

Culture Protocols

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Split Ratio 1:4
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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