Description:
EHLERS-DANLOS SYNDROME, FRIEDMAN-HARROD TYPE
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Repository
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NIGMS Human Genetic Cell Repository
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| Subcollection |
Heritable Diseases |
| Class |
Disorders of Connective Tissue, Muscle, and Bone |
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Cell Type
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Fibroblast
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Transformant
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Untransformed
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Race
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White
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Relation to Proband
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proband
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Confirmation
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Clinical summary/Case history
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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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| Passage Frozen |
4 |
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| IDENTIFICATION OF SPECIES OF ORIGIN |
Species of Origin Confirmed by Nucleoside Phosphorylase Isoenzyme Electrophoresis |
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| Remarks |
Severe hernias; mild joint hypermobility; asthmatic bronchitis; eczematoid dermatitis; severe scoliosis; died from ruptured aorta; similarly affected son; possible dominant inheritance |
| Friedman JM, Harrod MJ, An unusual connective tissue disease in mother and son: a "new" type of Ehlers-Danlos syndrome? Clin Genet21:168-73 1982 |
| PubMed ID: 7094393 |
| Passage Frozen |
4 |
| Split Ratio |
1:3 |
| Temperature |
37 C |
| Percent CO2 |
5% |
| 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 |
| Subcultivation Method |
trypsin-EDTA |
| Supplement |
- |
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