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TARDBP-related frontotemporal dementia

MedGen UID:
461519
•Concept ID:
C3150169
•
Disease or Syndrome
Synonyms: FRONTOTEMPORAL LOBAR DEGENERATION WITH TDP43 INCLUSIONS, TARDBP-RELATED; Frontotemporal lobar degeneration, TARDBP-related
 
Gene (location): TARDBP (1p36.22)
 
OMIM®: 612069

Recent clinical studies

Diagnosis

Clinical phenotypes and radiological findings in frontotemporal dementia related to TARDBP mutations.
Floris G, Borghero G, Cannas A, Di Stefano F, Murru MR, Corongiu D, Cuccu S, Tranquilli S, Cherchi MV, Serra A, Loi G, Marrosu MG, Chiò A, Marrosu F
J Neurol 2015 Feb;262(2):375-84. Epub 2014 Nov 20 doi: 10.1007/s00415-014-7575-5. PMID: 25408367

Supplemental Content

Table of contents

    Clinical resources

    Reviews

    Related information

    • ClinVar
      Related medical variations
    • Gene
      Related information in NCBI Gene
    • GTR
      Related information in GTR
    • GTR(Clinical)
      Clinical tests in GTR
    • OMIM
      Related records in OMIM
    • OMIM(Genes)
      OMIM records containing genes associated with phenotypes registered in MedGen

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