Document Detail


Cortical vascular abnormalities in the syndrome of celiac disease, epilepsy, bilateral occipital calcifications, and folate deficiency.
MedLine Citation:
PMID:  8363357     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
The pathological changes in the syndrome of celiac disease, folate deficiency, bilateral occipital calcifications, and intractable epilepsy have not been previously described. A child with this disorder had a field defect correlating with active lateralized epileptic discharges and asymmetrical lesions. After resection of the right occipital lobe she was seizure free for 4 years. A cortical vascular abnormality with patchy pial angiomatosis, fibrosed veins, and large jagged microcalcifications was found. These pathological abnormalities were similar though not identical to those found in the Sturge-Weber syndrome.
Authors:
A M Bye; F Andermann; Y Robitaille; M Oliver; T Bohane; E Andermann
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Publication Detail:
Type:  Case Reports; Journal Article    
Journal Detail:
Title:  Annals of neurology     Volume:  34     ISSN:  0364-5134     ISO Abbreviation:  Ann. Neurol.     Publication Date:  1993 Sep 
Date Detail:
Created Date:  1993-09-30     Completed Date:  1993-09-30     Revised Date:  2004-11-17    
Medline Journal Info:
Nlm Unique ID:  7707449     Medline TA:  Ann Neurol     Country:  UNITED STATES    
Other Details:
Languages:  eng     Pagination:  399-403     Citation Subset:  IM    
Affiliation:
Neurology Department, Prince of Wales Children's Hospital, Sydney, Australia.
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MeSH Terms
Descriptor/Qualifier:
Calcinosis / pathology*,  physiopathology,  psychology
Celiac Disease / pathology*,  physiopathology,  psychology
Child
Epilepsy / pathology*,  physiopathology,  psychology
Female
Folic Acid Deficiency / pathology*,  physiopathology,  psychology
Humans
Intelligence
Language
Magnetic Resonance Imaging
Memory
Occipital Lobe / pathology*
Syndrome
Visual Perception
Wechsler Scales

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


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