Huntington’s disease (HD) is an inherited neurodegenerative disorder caused by an expanded CAG repeat in the HTT gene. Genetic testing represents current routine standard in the diagnostic pathway of HD. However patients might be submitted to [18F]FDG PET to support the differential diagnosis of cognitive impairment or behavioral disturbances and might guide the subsequent work-up of the patient.

Case 12: Huntington’s Disease with Atypical Onset

Morbelli S.;
2021-01-01

Abstract

Huntington’s disease (HD) is an inherited neurodegenerative disorder caused by an expanded CAG repeat in the HTT gene. Genetic testing represents current routine standard in the diagnostic pathway of HD. However patients might be submitted to [18F]FDG PET to support the differential diagnosis of cognitive impairment or behavioral disturbances and might guide the subsequent work-up of the patient.
2021
2021 Case 10: Progressive Supranuclear Palsy (PSP). DOI: 10.1007/978-3-030-83598-9_10. In Clinical Nuclear Medicine in Neurology: an Atlas of Challenging Cases
Springer
59
63
DAT SPECT; Frontotemporal dementia; Huntington’s disease; Movement disorders; [; 18; F]FDG
Morbelli S.; Ferrarazzo G.
File in questo prodotto:
Non ci sono file associati a questo prodotto.

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2318/1965475
Citazioni
  • ???jsp.display-item.citation.pmc??? ND
  • Scopus 0
  • ???jsp.display-item.citation.isi??? ND
social impact