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Nonprogressive Familial Leukoencephalopathy With Porencephalic Cyst and Focal Seizures

Pediatric Neurology Unit Metabolic-Neurogenetic Clinic Wolfson Medical Center Holon, Israel

Nathan Watemberg, MD

Pediatric Neurology Unit Metabolic-Neurogenetic Clinic Wolfson Medical Center Holon, Israel

Dorit Lev, MD

Metabolic-Neurogenetic Clinic Genetics Institute Prenatal Neurology Clinic Wolfson Medical Center Holon, Israel

Gustavo Malinger, MD

Prenatal Neurology Clinic Wolfson Medical Center Holon, Israel

Yehudit Luckman, MD

Radiology Department Wolfson Medical Center Holon, Israel

Bruria Ben-Zeev, MD

Pediatric Neurology Unit Sheba Medical Center Ramat-Gan, Israel

Tally Lerman-Sagie, MD

Pediatric Neurology Unit Metabolic-Neurogenetic Clinc Prenatal Neurology Clinic Wolfson Medical Center Holon, Israel, asagie{at}post.tau.ac.il.

Two siblings with a similar white-matter disease but different clinical symptoms are described. The first sibling suffers from nonprogressive spastic hemiparesis secondary to a congenital periventricular porencephalic cyst. Her brother has focal epilepsy. On magnetic resonance imaging, both patients show diffuse white-matter involvement predominantly of the posterior periventricular area. We suggest that this is a familial white-matter disorder with minimal symptoms and no progression in early childhood. (J Child Neurol 2006;21:145—148; DOI 10.2310/7010.2006.00036).

Journal of Child Neurology, Vol. 21, No. 2, 145-148 (2006)
DOI: 10.1177/08830738060210021701


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