- Concept UI
- M0005800
- Scope Note
- A rare form of DEMENTIA that is sometimes familial. Clinical features include APHASIA; APRAXIA; CONFUSION; ANOMIA; memory loss; and personality deterioration. This pattern is consistent with the pathologic findings of circumscribed atrophy of the poles of the FRONTAL LOBE and TEMPORAL LOBE. Neuronal loss is maximal in the HIPPOCAMPUS, entorhinal cortex, and AMYGDALA. Some ballooned cortical neurons contain argentophylic (Pick) bodies. (From Brain Pathol 1998 Apr;8(2):339-54; Adams et al., Principles of Neurology, 6th ed, pp1057-9)
- Terms
-
Pick Disease of the Brain
Preferred Term
Term UI
T010821
Date06/18/1997
LexicalTag
EPO
ThesaurusID
-
Brain Atrophy, Circumscribed Lobar
Term UI
T369919
Date10/12/1999
LexicalTag
NON
ThesaurusID
NLM (2000)
-
Pick Disease
Term UI
T369920
Date10/12/1999
LexicalTag
EPO
ThesaurusID
NLM (2000)
-
Picks Disease of Brain
Term UI
T010822
Date03/18/1997
LexicalTag
EPO
ThesaurusID
NLM (1992)
-
Circumscribed Lobar Atrophy of the Brain
Term UI
T369917
Date10/12/1999
LexicalTag
NON
ThesaurusID
NLM (2000)
-
Pick's Disease
Term UI
T369921
Date10/12/1999
LexicalTag
EPO
ThesaurusID
-
Lobar Atrophy of the Brain
Term UI
T750418
Date05/04/2009
LexicalTag
NON
ThesaurusID
-
Dementia with Lobar Atrophy and Neuronal Cytoplasmic Inclusions
Term UI
T781527
Date12/02/2010
LexicalTag
NON
ThesaurusID
-
Pick Disease Of Brain
Term UI
T812127
Date11/15/2011
LexicalTag
NON
ThesaurusID
OMIM (2013)
-
Lobar Atrophy (Brain)
Term UI
T369918
Date10/12/1999
LexicalTag
NON
ThesaurusID
NLM (2000)
-
Lobar Atrophy Of Brain
Term UI
T812128
Date11/15/2011
LexicalTag
NON
ThesaurusID
OMIM (2013)