Abstract:
:A newborn with a rare type of lissencephaly is reported, characterized by extreme cerebral and cerebellar hypoplasia. The diagnosis was made by postmortem magnetic resonance imaging, indicating the value of such studies to evaluate neuronal migration disorders in patients in whom autopsy cannot be performed. Two earlier described microlissencephaly syndromes, the "Barth" and "McComb" type, are reviewed.
journal_name
Neuropediatricsjournal_title
Neuropediatricsauthors
Kroon AA,Smit BJ,Barth PG,Hennekam RCdoi
10.1055/s-2007-973778subject
Has Abstractpub_date
1996-10-01 00:00:00pages
273-6issue
5eissn
0174-304Xissn
1439-1899journal_volume
27pub_type
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