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Alzheimer Dementia, sporadic, association marker ACE |
AD2 |
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Signs/symptoms: |
Dementia, late onset, sporadic |
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Complications: |
Neuritic plaques and neurons with neurofibrillary tangles. |
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Early diagnosis/treatment: |
Yes |
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Association between homozygosity for both the ACE I and D allele polymorphisms and Alzheimer's disease (AD). |
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Material required: |
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Blood tubes: |
EDTA whole blood (do not freeze, do not centrifugate) |
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Mouth brush: |
Yes |
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Chromosomal localization: |
17q23 |
OMIM number: |
106180 |
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Angiotensin I converting enzyme (association marker) |
ACE |
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Gene regions tested: |
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Gene regions: |
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Amino acid positions: |
insertion/deletion polymorphism |
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Nucleotide positions: |
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Test methods: |
Sequencing |
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TP REVAL: |
250 |
TP Value: |
0.9 |
CHF |
225.00 |
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Other europe: |
EUR |
160.00 |
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Other regions: |
USD |
call |
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| De Bruin, T. W. A.; Mailly, F.; Van Barlingen, H. H. J. J.; Fisher, R.; Castro Cabezas, M.; Talmud, P.; Dallinga-Thie, G. M.; Humphries, S. E. Lipoprotein lipase gene mutations D9N and N291S in four pedigrees with familial combined hyperlipidaemia. Europ. J. Clin. Invest. 26: 631-639, 1996. | |
| Narain, Y.; Yip, A.; Murphy, T.; Brayne, C.; Easton, D.; Evans, J. G.; Xuereb, J.; Cairns, N.; Esiri, M. M.; Furlong, R. A.; Rubinsztein, D. C. The ACE gene and Alzheimer's disease susceptibility. J. Med. Genet. 37: 695-697, 2000. | |