Frontotemporal lobar degeneration with ubiquitin-positive inclusions

Developmental and genetic diseases

17q21.32 GeneReviews Google OMIM PubMed [Frontotemporal dementia]

*Gene map locus 17q21.32

Aphasia, primary progressive

Dementia, hereditary dysphasic disinhibition

FTDU

FTLD-TDP, GRN-related

FTLDU

Frontotemporal dementia, ubiquitin-positive

Frontotemporal lobar degeneration with TDP43 inclusions, GRN-related

HDDD

PPA

[Clinical features: frontotemporal dementia; neuronal degeneration with ubiquitin-positive, tau-negative inclusions in neurons of the second layer of the frontotemporal cortex and dentate gyrus of the hippocampus]

[Inheritance: autosomal dominant]

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A Belgian ancestral haplotype harbours a highly prevalent mutation for 17q21-linked tau-negative FTLD	A Belgian ancestral haplotype harbours a highly prevalent mutation for 17q21-linked tau-negative FTLD	A family with tau-negative frontotemporal dementia and neuronal intranuclear inclusions linked to chromosome 17
Brain	Brain	Brain


A family with tau-negative frontotemporal dementia and neuronal intranuclear inclusions linked to chromosome 17	A novel progranulin mutation associated with variable clinical presentation and tau, TDP43 and alpha-synuclein pathology	A novel progranulin mutation associated with variable clinical presentation and tau, TDP43 and alpha-synuclein pathology
Brain	Brain	Brain


A novel progranulin mutation associated with variable clinical presentation and tau, TDP43 and alpha-synuclein pathology	A novel progranulin mutation associated with variable clinical presentation and tau, TDP43 and alpha-synuclein pathology	A novel progranulin mutation associated with variable clinical presentation and tau, TDP43 and alpha-synuclein pathology
Brain	Brain	Brain


Familial frontotemporal dementia with ubiquitin-positive inclusions is linked to chromosome 17q21-22	Familial frontotemporal dementia with ubiquitin-positive inclusions is linked to chromosome 17q21-22	Familial frontotemporal dementia with ubiquitin-positive inclusions is linked to chromosome 17q21-22
Brain	Brain	Brain


Frontotemporal dementia and parkinsonism associated with the IVS1+1G-A mutation in progranulin: a clinicopathologic study	Frontotemporal dementia and parkinsonism associated with the IVS1+1G-A mutation in progranulin: a clinicopathologic study	Frontotemporal dementia and parkinsonism associated with the IVS1+1G-A mutation in progranulin: a clinicopathologic study
Brain	Brain	Brain

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Edited by Aldo Campana, August 21, 2012