Description:
EHLERS-DANLOS SYNDROME, TYPE VI
Repository
|
NIGMS Human Genetic Cell Repository
|
Subcollection |
Heritable Diseases |
Class |
Disorders of Connective Tissue, Muscle, and Bone |
Cell Type
|
Fibroblast
|
Transformant
|
Untransformed
|
Race
|
White
|
Family Member
|
2
|
Relation to Proband
|
sister
|
Confirmation
|
Clinical summary/Case history
|
Species
|
Homo sapiens
|
Common Name
|
Human
|
Remarks
|
|
Passage Frozen |
15 |
|
IDENTIFICATION OF SPECIES OF ORIGIN |
Species of Origin Confirmed by Nucleoside Phosphorylase Isoenzyme Electrophoresis |
|
procollagen-lysine 5-dioxygenase |
According to the submitter, biochemical test results for this subject showed decreased enzyme activity. EC Number: 1.14.11.4; 30% activity. |
|
Remarks |
Kyphoscoliosis; recurrent joint dislocation; hyperextensible skin and joints; decreased collagen hydroxylysine content; 30% of normal collagen lysyl hydroxylase activity |
Heikkinen J, Hautala T, Kivirikko KI, Myllyla R, Structure and expression of the human lysyl hydroxylase gene (PLOD): introns 9
and 16 contain Alu sequences at the sites of recombination in Ehlers-Danlos
syndrome type VI patients. Genomics24(3):464-71 1994 |
PubMed ID: 7713497 |
|
Hautala T, Heikkinen J, Kivirikko KI, Myllyla R, A large duplication in the gene for lysyl hydroxylase accounts for the type VI variant of Ehlers-Danlos syndrome in two siblings. Genomics15:399-404 1993 |
PubMed ID: 8449506 |
|
Quinn RS, Krane SM, Abnormal properties of collagen lysyl hydroxylase from skin fibroblasts of siblings with hydroxylysine-deficient collagen. J Clin Invest57:83-93 1976 |
PubMed ID: 173744 |
|
Pinnell SR, Krane SM, Kenzora JE, Glimcher MJ, A heritable disorder of connective tissue. Hydroxylysine-deficient collagen disease. N Engl J Med286:1013-20 1972 |
PubMed ID: 5016372 |
Passage Frozen |
15 |
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 |
- |
|
|