GM16510
Fibroblast from Skin, Unspecified
Description:
ADRENOLEUKODYSTROPHY, AUTOSOMAL NEONATAL FORM
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Repository
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NIGMS Human Genetic Cell Repository
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| Subcollection |
Heritable Diseases |
| Class |
Disorders of Steroid Metabolism |
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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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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 |
5 |
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| IDENTIFICATION OF SPECIES OF ORIGIN |
Species of Origin Confirmed by Nucleoside Phosphorylase,Glucose-6-Phosphate Dehydrogenase, and Lactate Dehydrogenase Isoenzyme Electrophoresis |
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| Remarks |
Clinically affected; dolichocephaly; prominent high forehead; epicanthal folds; broad nasal bridge; anteverted nostrils; mental retardation; seizures; the plasma concentration of C26:0 (ug/ml) is 4.6 times the mean of the normal control range; C16 and C18 plasmalogen levels are lower than normal; amounts of C26:0 and C26:1 and the ratio of C26/22 are higher than normal; deficient peroxisomal plasmalogen synthesis enzymes |
| Passage Frozen |
5 |
| 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 |
10% fetal bovine serum Not inactivated |
| Substrate |
None specified |
| Subcultivation Method |
trypsin-EDTA |
| Supplement |
- |
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