WOS: A1996WP95500012PubMed ID: 9107111It is generally accepted that there are two subsets of septo-optic dysplasia (deMorsier's syndrome), one with schizencephaly and the other without schizencephaly. A third form of the anomaly which is associated with callosal absence has also been described. Except for schizencephaly, the association of septo-optic dysplasia with another major type of disorder of neuronal migration and organization such as cortical dysplasia, has not yet been reported. We report the MR imaging examination of a 3-year-old patient with bilateral rolandic cortical dysplasia, and with apparent thinning of the optic nerves, and absent septum pellucidum (septo-optic dysplasia) as a new combination. This can be labelled as cort...
Schizencephaly is a rare central nervous system disorder with variable presentations. Here we report...
The clinical triad of septo-optic dysplasia (SOD) comprises the absence of the septum pellucidum, co...
Septo –optic dysplasia with lissencephaly rarely occurs simultaneously. We describe such a patient p...
ABSTRACT- Septo-optic dysplasia (SOD) is a syndrome composed by optic nerve and septum pellucidum dy...
Introduction: Septo-optic dysplasia (SOD) is an uncommon developmental disorder involving variable m...
Septo-optic dysplasia (SOD) is a syndrome composed by optic nerve and septum pellucidum dysgenesis. ...
PubMed ID: 8948159It is currently believed that there are two subsets of septo-optic dysplasia (de M...
WOS: A1996VT86300006PubMed ID: 8948159It is currently believed that there are two subsets of septo-o...
Objective: Septo-optic dysplasia consists of optic nerve and septum pellucidum dysgenesis. This synd...
Septo-optic dysplasia designates a unique and rare malformation of anterior midline structure of th...
Aim We set out to describe 17 patients with septo-optic dysplasia (SOD), focusing on the little-exp...
Three children with septo-optic dysplasia (SOD) and an associated malformation of cortical organizat...
The clinical triad of septo-optic dysplasia (SOD) comprises the absence of the septum pellucidum, co...
Septo-optic dysplasia (SOD) is a rare congenital disorder occurring in only 1 in 10,000 live births....
An 18-year-old male patient was admitted with loss of vision in the right eye and blurred vision in ...
Schizencephaly is a rare central nervous system disorder with variable presentations. Here we report...
The clinical triad of septo-optic dysplasia (SOD) comprises the absence of the septum pellucidum, co...
Septo –optic dysplasia with lissencephaly rarely occurs simultaneously. We describe such a patient p...
ABSTRACT- Septo-optic dysplasia (SOD) is a syndrome composed by optic nerve and septum pellucidum dy...
Introduction: Septo-optic dysplasia (SOD) is an uncommon developmental disorder involving variable m...
Septo-optic dysplasia (SOD) is a syndrome composed by optic nerve and septum pellucidum dysgenesis. ...
PubMed ID: 8948159It is currently believed that there are two subsets of septo-optic dysplasia (de M...
WOS: A1996VT86300006PubMed ID: 8948159It is currently believed that there are two subsets of septo-o...
Objective: Septo-optic dysplasia consists of optic nerve and septum pellucidum dysgenesis. This synd...
Septo-optic dysplasia designates a unique and rare malformation of anterior midline structure of th...
Aim We set out to describe 17 patients with septo-optic dysplasia (SOD), focusing on the little-exp...
Three children with septo-optic dysplasia (SOD) and an associated malformation of cortical organizat...
The clinical triad of septo-optic dysplasia (SOD) comprises the absence of the septum pellucidum, co...
Septo-optic dysplasia (SOD) is a rare congenital disorder occurring in only 1 in 10,000 live births....
An 18-year-old male patient was admitted with loss of vision in the right eye and blurred vision in ...
Schizencephaly is a rare central nervous system disorder with variable presentations. Here we report...
The clinical triad of septo-optic dysplasia (SOD) comprises the absence of the septum pellucidum, co...
Septo –optic dysplasia with lissencephaly rarely occurs simultaneously. We describe such a patient p...