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GM21640 Fibroblast from Skin, Unspecified

Description:

EHLERS-DANLOS SYNDROME, TYPE I; EDS1

Affected:

Yes

Sex:

Female

Age:

33 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 Unspecified
Cell Type Fibroblast
Tissue Type Skin
Transformant Untransformed
Sample Source Fibroblast from Skin, Unspecified
Family Member 1
Relation to Proband proband
Confirmation Molecular characterization before cell line submission to CCR
Species Homo sapiens
Common Name Human
Remarks Clinically affected; negative collagen I and III studies; iliac arterial dissection; several family members with aneurysms; affected brother is GM22034; joint pain; joint swelling in ankles; prominent forehead; epicanthal fold; malar hypoplasia; soft auricles; abnormal ear canals; micrognathia; wide palate; SM cleft; blue sclerae; pectus carinatum; pain and tenderness in abdomen; left and right carotid bruit; soft hyperextensible skin; cigarette paper and keliod scarring; easy bruising; piezogenic papules; hyperextension in shoulders, elbows, hips, knees and CMC, MCP, PIP and DIP joints; pes planus; genu valga; chokes in sleep; visual floaters; headaches; rib pain; urinary tract infections; mild disc disease at C4-C7; grade I spondylolisthesis in L5-S1 lumbar spine; disc extrusion at L4-S1; see GM21639 Lymphoid; molecular analysis of this donor subject with respect to the COL5A1 gene showed one allele as wild type and one allele with a G>A change in exon 52 (null allele)

Characterizations

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PDL at Freeze 6.65
Passage Frozen 2
 
IDENTIFICATION OF SPECIES OF ORIGIN Species of Origin confirmed by LINE assay
 

Phenotypic Data

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Remarks Clinically affected; negative collagen I and III studies; iliac arterial dissection; several family members with aneurysms; affected brother is GM22034; joint pain; joint swelling in ankles; prominent forehead; epicanthal fold; malar hypoplasia; soft auricles; abnormal ear canals; micrognathia; wide palate; SM cleft; blue sclerae; pectus carinatum; pain and tenderness in abdomen; left and right carotid bruit; soft hyperextensible skin; cigarette paper and keliod scarring; easy bruising; piezogenic papules; hyperextension in shoulders, elbows, hips, knees and CMC, MCP, PIP and DIP joints; pes planus; genu valga; chokes in sleep; visual floaters; headaches; rib pain; urinary tract infections; mild disc disease at C4-C7; grade I spondylolisthesis in L5-S1 lumbar spine; disc extrusion at L4-S1; see GM21639 Lymphoid; molecular analysis of this donor subject with respect to the COL5A1 gene showed one allele as wild type and one allele with a G>A change in exon 52 (null allele)

External Links

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NCBI GTR 130000 EHLERS-DANLOS SYNDROME, CLASSIC TYPE, 1; EDSCL1
OMIM 130000 EHLERS-DANLOS SYNDROME, CLASSIC TYPE, 1; EDSCL1
Omim Description EDS I
  EHLERS-DANLOS SYNDROME, CLASSIC SEVERE FORM
  EHLERS-DANLOS SYNDROME, GRAVIS TYPE
  EHLERS-DANLOS SYNDROME, TYPE I; EDS1

Culture Protocols

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Cumulative PDL at Freeze 6.65
Passage Frozen 2
Split Ratio 1:3
Temperature 37 C
Percent CO2 5%
Percent O2 AMBIENT
Medium Eagle's Minimum Essential Medium with Earle's salts and non-essential amino acids with 2mM L-glutamine or equivalent
Serum 15% fetal bovine serum Not inactivated
Substrate None specified
Supplement -
Pricing
International/Commercial/For-profit:
$373.00USD
U.S. Academic/Non-profit/Government:
$216.00USD
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