Document Detail


Wolfram syndrome presenting marked brain MR imaging abnormalities with few neurologic abnormalities.
MedLine Citation:
PMID:  17297000     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Wolfram syndrome is a rare autosomal recessive disorder featuring diabetes insipidus, diabetes mellitus, optic atrophy, and deafness; DIDMOAD is a commonly accepted anonym for this disorder. We describe a 35-year-old man with Wolfram syndrome, who had marked atrophy of the brain stem, middle cerebellar peduncle, and cerebellum. Despite these MR imaging findings involving the pontocerebellar tract, the patient had no neurologic abnormalities suggesting dysfunction of the brain stem or cerebellum. Patients with Wolfram syndrome may have discrepancies between neurologic and radiologic findings.
Authors:
S Ito; R Sakakibara; T Hattori
Publication Detail:
Type:  Case Reports; Journal Article    
Journal Detail:
Title:  AJNR. American journal of neuroradiology     Volume:  28     ISSN:  0195-6108     ISO Abbreviation:  AJNR Am J Neuroradiol     Publication Date:  2007 Feb 
Date Detail:
Created Date:  2007-02-13     Completed Date:  2007-04-03     Revised Date:  2008-02-14    
Medline Journal Info:
Nlm Unique ID:  8003708     Medline TA:  AJNR Am J Neuroradiol     Country:  United States    
Other Details:
Languages:  eng     Pagination:  305-6     Citation Subset:  IM    
Affiliation:
Department of Neurology, Graduate School of Medicine, Chiba University, Chiba, Japan.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Descriptor/Qualifier:
Adult
Cerebellum / pathology*
Humans
Magnetic Resonance Imaging*
Male
Optic Nerve / pathology
Pons / pathology*
Wolfram Syndrome / pathology*

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


Previous Document:  Dynamic 3D-CT angiography.
Next Document:  Imaging degeneration of the substantia nigra in Parkinson disease with inversion-recovery MR imaging...