ky7hblCxN1t2+/NXzTR91Y0jEkJnYn0hyzIF9dPsRLo/vLKUw9nMDc4Mnw+w57JssJs8x+2NNuO4O+yzLDO1+z5cc5wDTG5KN
WsZn7LliH3V6Cc/iUFZHC2H1CKlUqtpYWvsqnJIrI0zd+/+pbBXO4FZEpJMeBUnlOpoCCFrC5/+/RfwAq8Z/HZghdH
5Cc7uYgOHMRH/Etzw9p0P43Nv0lUgmnfW6zMDKJiIbepx/B4201/xaJojRYNN8pu++fhk1gH0ZD9EQ1To2HmAVEVTlhDPCNP0zaD
6hGIEHWCLyROExALjpGXoAL0TgrAXS4BUZxLulr///Lu/EpiCa5D3429cQBGJRw/EMKHjChNSYxJnp1YV4Ps2kYaU0cc+/Y
4yFZ7CNk65+cC3HqQ//x/ZE2NpE8bCtgfCLRuhYP2i4Pq906euRQ+uiy6PcGnZaZcjU8rKBkCKePTT/5Jrs9I1IAfyrz8+/HsS
很可能AD的可能性。只建议应用于科研或临床试验家族型类似症状的家族史,特别是经尸检诊断为AD易感基因(APP、PSEN1、PSEN2)证据增加AD病变可能性。此类型中APOE-4等位基因并无足够的特异
d4VbDKxwifgjW/T8HnUq/t9WNgtu1FfDIpw8+VNdf1Y7x/Cqzt+M/BP50app7hmfiMM2RS+Cju4bHGWa46Btcgf4a5/NxOwc++5