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Alzheimer disease, familial, 3, with spastic paraparesis and apraxia

MedGen UID:
334659
•Concept ID:
C1843015
•
Disease or Syndrome
Synonym: Alzheimer disease, type 3, with spastic paraparesis and apraxia
 
OMIM®: 104311; 607822

Recent clinical studies

Prognosis

Molecular evidence of presenilin 1 mutation in familial early onset dementia.
Matsubara-Tsutsui M, Yasuda M, Yamagata H, Nomura T, Taguchi K, Kohara K, Miyoshi K, Miki T
Am J Med Genet 2002 Apr 8;114(3):292-8. doi: 10.1002/ajmg.10250. PMID: 11920851

Clinical prediction guides

Molecular evidence of presenilin 1 mutation in familial early onset dementia.
Matsubara-Tsutsui M, Yasuda M, Yamagata H, Nomura T, Taguchi K, Kohara K, Miyoshi K, Miki T
Am J Med Genet 2002 Apr 8;114(3):292-8. doi: 10.1002/ajmg.10250. PMID: 11920851

Recent systematic reviews

A systematic review of familial Alzheimer's disease: Differences in presentation of clinical features among three mutated genes and potential ethnic differences.
Shea YF, Chu LW, Chan AO, Ha J, Li Y, Song YQ
J Formos Med Assoc 2016 Feb;115(2):67-75. Epub 2015 Aug 31 doi: 10.1016/j.jfma.2015.08.004. PMID: 26337232

Supplemental Content

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    Related information

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