Brown J
Department of Neurology, Addenbrooke's Hospital, Cambridge, UK.
Cell Mol Life Sci. 1998 Sep;54(9):925-7. doi: 10.1007/s000180050222.
Frontotemporal dementia accounts for a significant minority of all cases of presenile dementia. Many pedigrees have been described in which frontotemporal dementia is inherited as an autosomal dominant trait. Frontotemporal dementia is genetically heterogeneous with loci identified on chromosome 17 and chromosome 3. Clinical, pathological and genetic findings are described in a large Danish family in which the disease gene lies in the pericentromeric region of chromosome 3.
额颞叶痴呆在所有早老性痴呆病例中占相当比例。已经描述了许多家系,其中额颞叶痴呆作为常染色体显性性状遗传。额颞叶痴呆在基因上具有异质性,在17号染色体和3号染色体上已确定了相关基因座。在一个丹麦大家庭中描述了临床、病理和基因研究结果,该家庭的致病基因位于3号染色体的着丝粒周围区域。