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Hereditary porencephaly: clinical and MRI findings in two Dutch families.
- Source :
-
European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society [Eur J Paediatr Neurol] 2004; Vol. 8 (1), pp. 45-54. - Publication Year :
- 2004
-
Abstract
- Familial porencephaly is a rare disorder causing motor impairment, hemiplegia, mental retardation and epilepsy in variable degrees. Two families with porencephaly and apparently dominant inheritance are reported. Brain MRI findings are reviewed and described in seven affected individuals. Most patients also show white matter abnormalities in the cerebral hemisphere, also contralateral to the cystic lesion. In the first family an obligate carrier was identified who did not have a cystic lesion but clear abnormalities of the white matter. Although a predisposition for thrombophilia has previously been reported, we did not observe any genetic, environmental or epigenetic predisposition for the porencephaly. The lesions are most compatible with a deep venous thrombosis/ischemic event occurring in a late stage of pregnancy, not necessarily aggravated by perinatal asphyxia.
- Subjects :
- Adolescent
Adult
Brain pathology
Central Nervous System Cysts diagnosis
Cerebral Ventricles abnormalities
Cerebral Ventricles pathology
Child
Child, Preschool
Dominance, Cerebral genetics
Female
Follow-Up Studies
Genes, Dominant genetics
Humans
Infant
Male
Middle Aged
Netherlands
Neurologic Examination
Pedigree
Pregnancy
Thrombophilia diagnosis
Thrombophilia genetics
Tomography, X-Ray Computed
Brain abnormalities
Central Nervous System Cysts genetics
Magnetic Resonance Imaging
Subjects
Details
- Language :
- English
- ISSN :
- 1090-3798
- Volume :
- 8
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society
- Publication Type :
- Academic Journal
- Accession number :
- 15023374
- Full Text :
- https://doi.org/10.1016/j.ejpn.2003.10.002