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Journal of the Korean Society of Neonatology ; : 86-89, 1998.
Article in Korean | WPRIM | ID: wpr-126183

ABSTRACT

Schizencephaly, first described by Yakovlev and Wadsworth in 1946, is a rare congenital anomaly characterized by gray matter-lined clefts that extend through the entire cerebral hemisphere, from the ependymal lining of the lateral ventricle to the subarachnoid space. Clinically, patients with schizencephaly present motor dysfunction such as hemiparesis, seizures, and variable developmental delay. Absence of septum pellucidum, gray matter heterotopia, polymicrogyria, and hypoplasia of optic nerves were also frequently found to be associated with schizencephaly. We experienced a case of open-lip schizencephaly in a one-day-old male infant with wide, tense fontanel, which was confirmed by MRI.


Subject(s)
Humans , Infant , Male , Cerebrum , Lateral Ventricles , Lip , Magnetic Resonance Imaging , Malformations of Cortical Development , Optic Nerve , Paresis , Seizures , Septum Pellucidum , Subarachnoid Space , Transcutaneous Electric Nerve Stimulation
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