Results 1 to 10 of about 1,803 (152)

Complex neurological interplay: adult-onset migraine-triggered seizures in schizencephaly—a case report [PDF]

open access: yesFrontiers in Human Neuroscience
Schizencephaly is a rare congenital cerebral malformation typically diagnosed in early childhood due to serious neurological manifestations. Our case report described a patient with open lip schizencephaly, notable for three unique aspects.
Yuzhu Wang   +5 more
doaj   +4 more sources

Incidentally Identified Open‐Lip Schizencephaly in an Adult With Schizoaffective Disorder: A Case Report [PDF]

open access: yesClinical Case Reports
Open‐lip schizencephaly may remain undiagnosed until adulthood and can be incidentally identified during evaluation for unrelated presentations. This case highlights the coexistence of congenital neurodevelopmental abnormalities and schizoaffective ...
Saachi Bhattessa   +3 more
doaj   +3 more sources

Open lip schizencephaly: An unusual cause of hemiparesis: A case report [PDF]

open access: yesRadiology Case Reports
Schizencephaly is a highly uncommon clinical condition characterized by a diverse range of symptoms stemming from its numerous anatomical manifestations.
Melese Birara Mequanint   +3 more
doaj   +3 more sources

Undiagnosed Schizencephaly Presenting as Breakthrough Seizures [PDF]

open access: yesClinical Practice and Cases in Emergency Medicine
Case Presentation: A 19-year-old male presented for evaluation of breakthrough seizures after inability to refill his medication following recent immigration from Haiti. Previously, the patient had never received neuroimaging due to financial constraints
John Coacci, Peter Viccellio
doaj   +4 more sources

A unilateral open-lip schizencephaly in a neonate: A rare case report [PDF]

open access: yesRadiology Case Reports
Schizencephaly is a rare congenital central nervous system (CNS) developmental disorder characterized by abnormal cleft extending from the lateral ventricles to the cerebral cortex.
Seth Kwadjo Angmorterh, PhD   +13 more
doaj   +2 more sources

Unilateral schizencephaly open lip with septo optic dysplasia in adult woman with glaucoma: A rare case [PDF]

open access: yesRadiology Case Reports
This case report presents a 38-year-old female with unilateral open-lip schizencephaly coexisting with septo-optic dysplasia. The patient lacked motor deficits, maintaining normal developmental milestones.
Eppy Buchori Aristiady   +2 more
doaj   +2 more sources

Rare encounter: Adult-onset temporal lobe schizencephaly with septo-optic dysplasia - a case report on comprehensive diagnosis and management [PDF]

open access: yesRadiology Case Reports
This case report presents a 21-year-old male with recurrent seizures attributed to isolated temporal lobe closed-lip schizencephaly coexisting with septo-optic dysplasia. Despite adult-onset seizures, the patient lacked motor deficits, maintaining normal
Sundar Suwal, MD   +6 more
doaj   +2 more sources

Subependymal Gray Matter Heterotopia With Seizure in a 6‐Month‐Old Child [PDF]

open access: yesClinical Case Reports
A 6‐month‐old male presented with seizures. Non‐contrast CT revealed subependymal gray matter heterotopia, corpus callosum dysgenesis, colpocephaly, and suspicious closed‐lip bilateral parieto‐occipital schizencephaly.
Bibek Shrestha   +3 more
doaj   +2 more sources

Schizencephaly: A rare cause of late-onset epilepsy in an adult [PDF]

open access: yesRadiology Case Reports, 2023
Schizencephaly, a rare congenital cerebral deformity that affects the cerebral mantle and is caused by both hereditary and acquired factors, is defined by a cleft that spans the entire cerebral hemisphere from the lateral ventricle to the cerebral cortex.
Khadija Laasri, MD   +7 more
doaj   +2 more sources

Open Lip Schizencephaly Misdiagnosed as Paralytic Poliomyelitis in an 85‐Year‐Old: A Case Report [PDF]

open access: yesClinical Case Reports
The variable clinical presentations of open lip schizencephaly can lead to misdiagnosis, as occurred in this case originally misdiagnosed as polio in the 1930s.
Zihan Guo   +2 more
doaj   +2 more sources

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