Neuroimaging findings in late infantile GM1 gangliosidosis.

Publication/Presentation Date

10-1-1998

Abstract

Late infantile GM1 gangliosidosis is an extremely rare metabolic disorder with clinical features of seizure and progressive motor and mental retardation without facial dysmorphism or visceral organomegaly. We report the CT and MR imaging findings in one infant, which included abnormalities of the cerebral cortex, white matter, and deep nuclei.

Volume

19

Issue

9

First Page

1628

Last Page

1630

ISSN

0195-6108

Disciplines

Diagnosis | Medicine and Health Sciences | Other Analytical, Diagnostic and Therapeutic Techniques and Equipment | Radiology

PubMedID

9802482

Department(s)

Department of Radiology and Diagnostic Medical Imaging

Document Type

Article

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