Alzheimer disease 13

Alzheimer disease 13 is a rare form of Alzheimer disease that is associated with a variation in the region 1q21. This condition has been noted to be linked with the gene AD13 and is identified in specialized databases under OMIM and GARD. The information available focuses on the genetic association and the uncommon nature of this disease, which distinguishes it from more common Alzheimer disease types. This summary is based on limited available data from trusted sources. Researchers have noted that variations in specific regions of the genome may contribute to the distinct characteristics of Alzheimer disease 13. Although details are still evolving, the diagnosis of this condition typically involves recognizing its genetic markers, and further studies may help clarify its full features and progression over time.

Information about symptoms is currently limited for this condition.

Alzheimer disease 13 has a genetic component as it is associated with a variation in the region 1q21 and involves the AD13 gene. The available data suggests that changes in this area of the genome are related to the condition, although detailed mechanisms and additional risk factors are not fully established from currently available sources.

Information about treatment is currently limited for this condition.

Information about prognosis is currently limited for this condition.

Information about research is currently limited for this condition.