SPECT, CT and MRI in a Turkish family with huntington's disease

Autor:	A. R. Rozeboom, F. Barkhof, R. P. M. Bruyn, J.A.G. Geelen, F. A. van der Weel, G. Hageman, P. Scheltens
Rok vydání:	1993
Předmět:	Adult Male congenital hereditary and neonatal diseases and abnormalities medicine.medical_specialty Neurology Single-photon emission computed tomography Asymptomatic Huntington's disease medicine Humans Radiology Nuclear Medicine and imaging Neuroradiology Tomography Emission-Computed Single-Photon medicine.diagnostic_test business.industry Brain Magnetic resonance imaging Chorea medicine.disease Magnetic Resonance Imaging Pedigree Huntington Disease Regional Blood Flow Positron emission tomography Female Neurology (clinical) Radiology Atrophy medicine.symptom Tomography X-Ray Computed Cardiology and Cardiovascular Medicine business Nuclear medicine
Zdroj:	Neuroradiology. 35:525-528
ISSN:	1432-1920 0028-3940
DOI:	10.1007/bf00588713
Popis:	A Turkish family with Huntington's disease documented on CT, MRI and SPECT is reported. Whereas in clinically definite cases CT and MRI are of limited value and SPECT does not add anything of value, in one asymptomatic subject SPECT showed moderate caudate nucleus hypoperfusion, underlining the hypothesis that SPECT may have a role in predicting Huntington's disease.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f267c9d4a21620f7a9cc45c4afc79c54 https://doi.org/10.1007/bf00588713 Zobrazit plný text záznamu Full text from SpringerLink