GM16391
Fibroblast from Skin, Unspecified
Description:
TRICHOTHIODYSTROPHY; TTD ICHTHYOSIFORM ERYTHRODERMA WITH HAIR ABNORMALITY AND MENTAL AND GROWTH RETARDATION, INCLUDED
Repository
|
NIGMS Human Genetic Cell Repository
|
Subcollection |
Heritable Diseases |
Class |
Disorders of Connective Tissue, Muscle, and Bone |
Class |
Repair Defective and Chromosomal Instability Syndromes |
Biopsy Source
|
Unspecified
|
Cell Type
|
Fibroblast
|
Tissue Type
|
Skin
|
Transformant
|
Untransformed
|
Sample Source
|
Fibroblast from Skin, Unspecified
|
Race
|
White
|
Ethnicity
|
WELSH
|
Relation to Proband
|
proband
|
Confirmation
|
Clinical summary/Case history
|
Species
|
Homo sapiens
|
Common Name
|
Human
|
Remarks
|
|
IDENTIFICATION OF SPECIES OF ORIGIN |
Species of Origin Confirmed by Nucleoside Phosphorylase,Glucose-6-Phosphate Dehydrogenase, and Lactate Dehydrogenase Isoenzyme Electrophoresis |
|
Remarks |
Clinically affected; low birth weight; short stature; impaired development; skin of trunk ichthyotic; scalp hair short and coarse; elfinlike facies with a beaked nose, receding chin, and large protruding ears; big toenails show lateral ridging; ataxic gait; microscopic exam of hair revealed striking transverse bandlike defects under polarized light and trichorrhexis nodosalike transverse fractures of the hair shafts; electron microscopy demonstrated ridging and fluting along the hair shaft with loss of normal pattern of cuticular scales; amino acid analysis of hair samples showed reduced cystine content (4.6% compared to 8.4% in normal control); abnormally low unscheduled DNA synthesis induced by UVC irradiation and bulk of recovery of RNA synthesis after UVC irradiation |
Split Ratio |
1:2 |
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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