Results 91 to 100 of about 309,057 (256)
Arnold Chiari is a congenitally developed malformation. Syringomyelia is accompanied in some of the cases. Four types of malformation have been identified and type I is frequent in adults. Cerebellar tonsils are displaced downward from the foramen magnum
Mukadder Sanli +5 more
doaj +1 more source
The clinical manifestations of PFO. Although the majority of PFOs are benign and asymptomatic, they can present with a variety of clinical manifestations, or coexisting with other diseases and aggravating their symptoms, including cerebral diseases (such as CS, epilepsy, TIA, or migraine), systemic embolism (such as embolism in renal artery, coronary ...
Linlin Meng +6 more
wiley +1 more source
Intermittent symptoms of obstructive hydrocephalus in a young woman with Chiari-I malformation are reported from the Neuro-Ophthalmology Service, Wills Eye Hospital, Philadelphia ...
J Gordon Millichap
core +1 more source
We report a case of a 22‐year‐old woman with predominantly cutaneous involvement in whom whole‐exome sequencing from both blood‐ and hair‐derived DNA samples identified somatic mosaicism for the rare HRAS p.Gly13Asp variant. This case expands the phenotypic spectrum of Costello syndrome and underscores the importance of multitissue genomic analysis ...
Jovan Lalosevic +6 more
wiley +1 more source
Background Chiari syndrome is a very rare cause of secondary trigeminal neuralgia (TN). There are a few cases of TN associated with Chiari syndrome in the literature, and all of these cases were reported as Chiari type 1.
Ahmet Cemil Ergün +3 more
doaj +1 more source
Cerebellar cognitive affective syndrome related to chiari malformation: a case report
Numerous studies have showed that the cerebellum has a role in processing higher brain functions besides motor coordination. Various types of congenital lesions of cerebellum are associated with neuropsychological impairments and behavioral changes.
Gokben Hızlı Sayar +4 more
doaj +1 more source
ABSTRACT Objectives To describe, characterize and determine the frequency of interhemispheric fissure (IHF) distortion on ultrasound in fetuses with open spina bifida (OSB), evaluate its association with other intracranial findings and biometric parameters and assess its evolution after prenatal closure of the spinal defect.
L. S. Carmant +7 more
wiley +1 more source
Chiari I Malformation Associated with Turner Syndrome
Turner syndrome (TS) is a rare genetic disease due to the absence of one X chromosome. Patients with TS have more subtle neurological/neuropsychiatric problems, while headache is an uncommon clinical presentation which needs attention.
Jeevan S. Nair +1 more
core +1 more source
Manajemen Anestesi pada Pasien dengan Chiari Malformation dan Syringomyelia
Latar belakang: Chiari malformation merupakan kelainan anatomi dari otak kecil dimana tonsil cerebellum turun ke arah Foramen magnum dan menimbulkan serangkaian gejala klinis.
Tomas Ari Kurniawan, I Ketut Sinardja
doaj +1 more source
Object Symptomatic pediatric Chiari malformation Type I (CM-I) is most often treated with posterior fossa decompression (PFD), but controversy exists over whether the dura needs to be opened during PFD.
Benjamin C. Kennedy +6 more
semanticscholar +1 more source

