SwePub
Sök i LIBRIS databas

  Extended search

onr:"swepub:oai:gup.ub.gu.se/83180"
 

Search: onr:"swepub:oai:gup.ub.gu.se/83180" > Microdysgenesis in ...

  • 1 of 1
  • Previous record
  • Next record
  •    To hitlist

Microdysgenesis in surgical specimens from patients with epilepsy: occurrence and clinical correlations.

Nordborg, Claes, 1946 (author)
Gothenburg University,Göteborgs universitet,Institutionen för laboratoriemedicin , Avdelningen för patologi,Institute of Laboratory Medicine, Dept of Pathology
Eriksson, s (author)
Rydenhag, Bertil, 1954 (author)
Gothenburg University,Göteborgs universitet,Institutionen för klinisk neurovetenskap,Institute of Clinical Neurosciences
show more...
Uvebrant, Paul, 1951 (author)
Gothenburg University,Göteborgs universitet,Institutionen för kvinnors och barns hälsa, Avdelningen för pediatrik,Institute for the Health of Women and Children, Dept of Paediatrics
Malmgren, Kristina, 1952 (author)
Gothenburg University,Göteborgs universitet,Institutionen för klinisk neurovetenskap,Institute of Clinical Neurosciences
show less...
 (creator_code:org_t)
1999
1999
English.
In: Journal of neurology, neurosurgery, and psychiatry. - 0022-3050. ; 67:4, s. 521-4
  • Journal article (peer-reviewed)
Abstract Subject headings
Close  
  • Malformations of cortical development are commonly associated with epilepsy. In the first 139 consecutive patients in the G?teborg epilepsy surgery series, parenchymal malformations were found in 56. 1% of the children and in 23.1% of the adults. Microdysgenesis (MDG), which was the most common parenchymal malformation, was found in 35. 1% of the children and in 16.7% of the adults. The aim of this study was to identify clinical characteristics of patients with MDG. Mental retardation was found to be significantly more common in patients with major parenchymal malformations and in patients with MDG compared with patients without parenchymal malformations. Patients with major parenchymal malformations as well as patients with MDG also had a significantly earlier onset of seizures than patients without parenchymal malformations, also when adjusting for mental retardation. Patients with MDG were in these clinical aspects shown to closely resemble patients with major malformations. These findings suggest that MDG is a pathoanatomical entity of clinical relevance, with implications both in mental retardation and in epileptogenesis.

Keyword

Adolescent
Adult
Aged
Cerebral Cortex
abnormalities
pathology
Child
Child
Preschool
Epilepsy
pathology
Female
Humans
Male
Middle Aged
Neurons
pathology

Publication and Content Type

ref (subject category)
art (subject category)

Find in a library

To the university's database

  • 1 of 1
  • Previous record
  • Next record
  •    To hitlist

Search outside SwePub

Kungliga biblioteket hanterar dina personuppgifter i enlighet med EU:s dataskyddsförordning (2018), GDPR. Läs mer om hur det funkar här.
Så här hanterar KB dina uppgifter vid användning av denna tjänst.

 
pil uppåt Close

Copy and save the link in order to return to this view