Document Detail


Infantile neuroaxonal dystrophy: neuroradiological studies in 11 patients.
MedLine Citation:
PMID:  10379598     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
We report the imaging findings in 11 patients with infantile neuroaxonal dystrophy. Ten patients underwent 15 MRI examinations; one patient had only CT. Of the ten patients who underwent MRI, eight had cerebellar atrophy and mildly increased signal from the cerebellar cortex on T2-weighted images. With T2 weighting there was slightly increased signal from the dentate nuclei in two patients and from the posterior periventricular white matter in three. We saw four patients with a thin optic chiasm. The only two brothers in the series had markedly low signal from the globus pallidus and substantia nigra on 1.5 T T2-weighted images, as seen in Hallervorden-Spatz disease (HSD). Abnormalities of the globus pallidus may be related to a protracted course of the disease. However, an overlap with HSD should be considered.
Authors:
L Farina; N Nardocci; M G Bruzzone; L D'Incerti; G Zorzi; L Verga; M Morbin; M Savoiardo
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Publication Detail:
Type:  Journal Article    
Journal Detail:
Title:  Neuroradiology     Volume:  41     ISSN:  0028-3940     ISO Abbreviation:  Neuroradiology     Publication Date:  1999 May 
Date Detail:
Created Date:  1999-08-17     Completed Date:  1999-08-17     Revised Date:  2004-11-17    
Medline Journal Info:
Nlm Unique ID:  1302751     Medline TA:  Neuroradiology     Country:  GERMANY    
Other Details:
Languages:  eng     Pagination:  376-80     Citation Subset:  IM    
Affiliation:
Department of Neuroradiology, Istituto Nazionale Neurologico C. Besta, Milan, Italy.
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MeSH Terms
Descriptor/Qualifier:
Brain / pathology
Child
Child, Preschool
Female
Humans
Infant
Magnetic Resonance Imaging*
Male
Neuroaxonal Dystrophies / diagnosis*

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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