Presenilin 1 and APP Gene Mutations in Early-Onset AD Families from a Southeast Region of China.

BACKGROUND

Early-Onset Familial Alzheimer's Disease (EOFAD) has been reported to be associated with Presenilin 1 (PSEN1), Presenilin 2 (PSEN2), and Amyloid Precursor Protein (APP) genes. The spectrum of mutations in Chinese patients with EOFAD was rarely investigated.

OBJECTIVE

To investigate the spectrum of mutations in patients with EOFAD in Chinese population.

METHODS

We performed whole-exome sequencing and described relevant clinical features in a total of 67 subjects from 3 families with EOFAD.

RESULTS

A splice mutation (p.S290C) in PSEN1 and a missense mutation (p.V717I) in APP were identified.

CONCLUSION

The variant p. S290C (c.869-2>G) in PSEN1 in Chinese EOAD family revealed different clinical phenotypes when compared with that of Europeans.