Results 31 to 40 of about 6,027 (196)

Association of Quality of Life Domains and Clinical Symptoms in Patients With Familial Cerebral Cavernous Malformation. [PDF]

open access: yesJ Am Heart Assoc
Background Familial cerebral cavernous malformation (fCCM) is characterized by multiple brain lesions affecting quality of life. PROMIS‐29 (Patient‐Reported Outcomes Measurement Information System 29) is a quality of life survey validated in some ...
Tsang C   +13 more
europepmc   +2 more sources

Multiple cerebral cavernous malformations in a pediatric patient with Turner syndrome

open access: yesInterdisciplinary Neurosurgery, 2017
Turner syndrome (TS; 45,X0) is a relatively common chromosomal disorder that is associated with characteristic phenotypic stigmata: short stature, webbed neck, broad (“shield”) chest with widely spaced nipples, cubitus valgus, ovarian dysgenesis (“streak
Nicholas T. Gamboa, B.S.   +4 more
doaj   +1 more source

The cerebral cavernous malformations proteins

open access: yesOncotarget, 2015
Inherited mutations in three genes lead to the familial form of Cerebral Cavernous Malformations (CCM). These vascular dysplasias most commonly occur in the brain, and manifest as dilated, mulberry-shaped lesions with a single endothelial layer. The consequences of these lesions can be leakage and sequelae such as focal neurological deficits, epilepsy,
Xiaofeng, Li   +2 more
openaire   +2 more sources

Familial Multiple Cavernous Malformation Syndrome: MR Features in This Uncommon but Silent Threat

open access: yesJournal of the Belgian Society of Radiology, 2016
Cerebral cavernous malformations (CCM) are vascular malformations in the brain and spinal cord. The familial form of cerebral cavernous malformation (FCCM) is uncommon.
Marc Mespreuve   +2 more
doaj   +1 more source

Intraoperative MRI-assisted neuro-port surgery for the resection of cerebral intraparenchymal cavernous malformation

open access: yesChinese Neurosurgical Journal, 2019
Background Intraparenchymal cerebral cavernous malformation is difficult to localize intraoperatively with conventional frameless navigation due to the “brain shift” effect.
Min Zhao   +4 more
doaj   +1 more source

Cavernous malformation hemorrhage due to trans-mural pressure alterations after cerebrospinal fluid diversion: a case report

open access: yesBMC Neurology, 2020
Background Cavernous malformations are rare cerebral pseudo-vascular lesions with annualized bleeding rates of 0.5–3% in most studies. Of the various explored risk factors for bleeding to date, only prior hemorrhage has shown significant correlation ...
Benjamin R. Hartley   +2 more
doaj   +1 more source

Contralateral Anterior Interhemispheric–Transcallosal–Transrostral Approach for the Resection of a Subcallosal Cavernous Malformation: A Case Report and an Operative Video

open access: yesFrontiers in Surgery, 2022
This case report demonstrates the surgical resection of a cerebral cavernous malformation located in the subcallosal region. The authors present a detailed operative video explaining the steps to successfully remove the lesion through a contralateral ...
Aderaldo Costa Alves   +3 more
doaj   +1 more source

Coexistence of Cerebral Calcified Cavernous Malformation and Developmental Venous Anomaly

open access: yes, 2020
Cerebral cavernous malformations are common vascular malformation of the central nervous system. It may cause various symptoms, such as seizures, intracranial hemorrhage, but most are asymptomatic and diagnosed incidentally. The authors present a case of
Fahri Aydin   +3 more
core   +1 more source

Familial cerebral cavernous malformations: Rio de Janeiro study and review of the recommendations for management Malformação cavernosa cerebral familiar: um estudo no Rio de Janeiro e revisão das recomendações para tratamento

open access: yesArquivos de Neuro-Psiquiatria, 2008
OBJECTIVE: Multiple cerebral cavernous malformation (CCM) is the hallmark of familial presentation of cavernous malformation in the brain. We describe an ongoing Familial Cerebral Cavernous Malformation Project in the Rio de Janeiro state showing genetic
Flávio Domingues   +7 more
doaj   +1 more source

CEREBRAL CAVERNOUS MALFORMATION COEXISTING WITH PITUITARY ADENOMA, HASHIMOTO THYROIDITIS AND MENTAL ILLNESS: FIRST CASE REPORT.

open access: yes, 2017
Cerebral Cavernous Malformations (CCMs) are vascular lesions involving brain capillaries. They may occur sporadically or be inherited as autosomal dominant character.
Sara Guido
core   +1 more source

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