GM21640
Fibroblast from Skin, Unspecified
Description:
EHLERS-DANLOS SYNDROME, TYPE I; EDS1
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Repository
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NIGMS Human Genetic Cell Repository
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| Subcollection |
Heritable Diseases |
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Biopsy Source
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Unspecified
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Cell Type
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Fibroblast
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Tissue Type
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Skin
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Transformant
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Untransformed
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Sample Source
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Fibroblast from Skin, Unspecified
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Family Member
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1
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Relation to Proband
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proband
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Confirmation
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Molecular characterization before cell line submission to CCR
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Species
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Homo sapiens
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Common Name
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Human
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Remarks
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| PDL at Freeze |
6.65 |
| Passage Frozen |
2 |
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| IDENTIFICATION OF SPECIES OF ORIGIN |
Species of Origin confirmed by LINE assay |
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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) |
| 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 |
- |
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