Mutations in genes encoding APP (amyloid precursor protein), presenilin 1 and 2 (PS1 and PS2 respectively), as well as ε4 allele of Apolipoprotein E are reported to be linked to rare familial and early development of AD (Selkoe, 2001a,b; Scheltens et al., 2016). The gene discussed is APP; the disease is Alzheimer disease.