Lipoma of the Corpus callosum: Report of a Case and Review of the Literature

1979 ◽  
Vol 5 (5) ◽  
pp. 476-483 ◽  
Author(s):  
Tatsunori Suemitsu ◽  
Shun-Ichi Nakajima ◽  
Katsuko Kuwajima ◽  
Kenji Nihei ◽  
Shigehiko Kamoshita
Keyword(s):  
Corpus Callosum ◽  
Review Of The Literature

Ivemark syndrome with agenesis of the corpus callosum: a case report with a review of the literature

2002 ◽  
Vol 22 (11) ◽  
pp. 1011-1015 ◽  
Author(s):  
F. Noack ◽  
F. Sayk ◽  
A. Ressel ◽  
C. Berg ◽  
U. Gembruch ◽  
...  
Keyword(s):  
Case Report ◽  
Corpus Callosum ◽  
Review Of The Literature ◽  
Ivemark Syndrome

Calcifying pseudoneoplasm of the neuraxis overlying the corpus callosum: a case report and review of the literature

2013 ◽  
Vol 32 (11) ◽  
pp. 515-521 ◽  
Author(s):  
Matthew Grabowski ◽  
Pablo Recinos ◽  
Tsulee Chen ◽  
Richard Prayson ◽  
Michael Vogelbaum
Keyword(s):  
Case Report ◽  
Corpus Callosum ◽  
Review Of The Literature

scholarly journals Alien hand syndrome following corpus callosum infarction: A case report and review of the literature

2016 ◽  
Vol 12 (4) ◽  
pp. 2129-2135 ◽  
Author(s):  
Xiaoyu Gao ◽  
Bing Li ◽  
Wenzheng Chu ◽  
Xuwen Sun ◽  
Chunjuan Sun
Keyword(s):  
Case Report ◽  
Corpus Callosum ◽  
Review Of The Literature ◽  
Alien Hand Syndrome ◽  
Alien Hand

A New Case with Corpus Callosum Abnormalities, Microcephaly and Seizures Associated with a 2.3-Mb 1q43-q44 Deletion

2019 ◽  
Vol 159 (3) ◽  
pp. 126-129 ◽  
Author(s):  
Elisabet Lloveras ◽  
Anna Canellas ◽  
Laura Barranco ◽  
Claudia Alves ◽  
Marta Vila-Real ◽  
...  
Keyword(s):  
Corpus Callosum ◽  
Developmental Delay ◽  
Facial Dysmorphism ◽  
Review Of The Literature ◽  
Expressive Speech ◽  
Genetic Causes ◽  
Chromosome 1Q ◽  
Rare Syndrome

1q44 deletion is a rare syndrome associated with facial dysmorphism and developmental delay, in particular related with expressive speech, seizures, and hypotonia (ORPHA:238769). Until today, the distinct genetic causes for the different symptoms remain not entirely clear. We present a patient with a 2.3-Mb 1q44 deletion, including AKT3, ZBTB18, and HNRNPU, who shows microcephaly, developmental delay, abnormal corpus callosum, and seizures. The genetic findings in this case and a review of the literature spotlight a region between 243 Mb and 245 Mb on chromosome 1q related to the genesis of the typical symptoms of 1q44 deletion.

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