scholarly journals Cavernous Angioma of the Corpus Callosum Mimicking an Astrocytic Tumor. Case Report.

2001 ◽  
Vol 41 (7) ◽  
pp. 349-351 ◽  
Author(s):  
Shunichi HARADA ◽  
Maki NIIMI ◽  
Kenichi MURAKAMI ◽  
Tsuneo NAKAMURA
Keyword(s):  
Case Report ◽  
Corpus Callosum ◽  
Cavernous Angioma ◽  
Astrocytic Tumor

Absence of corpus callosum – A case report

2015 ◽  
Vol 64 ◽  
pp. S49
Author(s):  
Deb Barma Saranya ◽  
J. Sarma ◽  
K.L. Talukdar
Keyword(s):  
Case Report ◽  
Corpus Callosum

Callosal disconnection syndrome after ischemic stroke of the corpus callosum due to meningococcal meningitis: A case report

2016 ◽  
Vol 369 ◽  
pp. 119-120 ◽  
Author(s):  
Nicola A. Marchi ◽  
Radek Ptak ◽  
Corinne Wetzel ◽  
Maria I. Vargas ◽  
Armin Schnider ◽  
...  
Keyword(s):  
Ischemic Stroke ◽  
Case Report ◽  
Corpus Callosum ◽  
Meningococcal Meningitis ◽  
Disconnection Syndrome

F076 A case report of auditory neuropathy with agenesis of the corpus callosum

2011 ◽  
Vol 75 ◽  
pp. 97
Author(s):  
B.-H. Chou ◽  
T.-T. Yen ◽  
J.-Y. Shiao ◽  
R.-S. Jiang ◽  
C.-M. Chiang ◽  
...  
Keyword(s):  
Case Report ◽  
Corpus Callosum ◽  
Auditory Neuropathy

scholarly journals Lissencephaly, abnormal genitalia and refractory epilepsy: case report of XLAG syndrome

2006 ◽  
Vol 64 (4) ◽  
pp. 1023-1026 ◽  
Author(s):  
Mônica Jaques Spinosa ◽  
Paulo Breno Noronha Liberalesso ◽  
Simone Carreiro Vieira ◽  
Alaídes Susana Fojo Olmos ◽  
Alfredo Löhr Júnior
Keyword(s):  
Case Report ◽  
Corpus Callosum ◽  
Refractory Epilepsy ◽  
Genetic Disorder ◽  
Ductus Arteriosus ◽  
Ambiguous Genitalia ◽  
Second Child ◽  
Neonatal Onset ◽  
The Right ◽  
Male Genotype

INTRODUCTION: X-linked lissencephaly with ambiguous genitalia (XLAG) is a recently described genetic disorder caused by mutation in the aristaless-related homeobox (ARX) gene (Xp22.13). Patients present with lissencephaly, agenesis of the corpus callosum, refractory epilepsy of neonatal onset, acquired microcephaly and male genotype with ambiguous genitalia. CASE REPORT: Second child born to healthy nonconsanguineous parents, presented with seizures within the first hour of life that remained refractory to phenobarbital, phenytoin and midazolam. Examination identified microcephaly, axial hypotonia, pyramidal signs and ambiguous genitalia. EEG showed disorganized background activity and seizures starting at the right midtemporal, central and occipital regions. MRI showed diffuse pachygyria, moderate thickening of the cortex, enlarged ventricles, agenesis of the corpus callosum and septum pellucidum. Karyotype showed a 46,XY genotype. Additional findings were hypercalciuria, vesicoureteral reflux, patent ductus arteriosus and chronic diarrhea.

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