Printer-friendly version

Alzheimer Dementia, sporadic, association marker ACE

Geriatry 13.003

Alzheimer Dementia, sporadic, association marker ACE

AD2

Signs/symptoms: Dementia, late onset, sporadic
Complications: Neuritic plaques and neurons with neurofibrillary tangles.
Early diagnosis/treatment: Yes
Association between homozygosity for both the ACE I and D allele polymorphisms and Alzheimer's disease (AD).

Material required:

Blood tubes: EDTA whole blood (do not freeze, do not centrifugate)
Mouth brush: Yes
Chromosomal localization: 17q23 OMIM number: 106180

Angiotensin I converting enzyme (association marker)

ACE

Gene regions tested:

Gene regions:
Amino acid positions: insertion/deletion polymorphism
Nucleotide positions:
Test methods: Sequencing

Prices:

Switzerland:

8820.00 8811.01 8819.01
  TP REVAL: 250 TP Value: 0.9 CHF 225.00
Other europe: EUR 160.00
Other regions: USD call

References:

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.

Browse Gene Tests

To view all our gene tests, please visit our Test Menu.