Results 1 to 10 of about 5,326 (134)

Morphometric assessment of the posterior cranial fossa and its contents in patients with chiari malformation type I and type 0 [PDF]

open access: yesActa Neurochirurgica
Background Chiari Malformation Type I and Type 0 are congenital malformations diagnosed by MRI findings of at least 5 mm and less than 3 mm of cerebellar ectopy below the foramen magnum respectively.
Busra Candan, Birol Ozkal, Esra Top
doaj   +2 more sources

Pediatric triad of craniofacial fibrous dysplasia, Chiari malformation type I and syringomyelia: a case report [PDF]

open access: yesActa Neurochirurgica
Fibrous dysplasia is a benign bone disease characterized by the replacement of normal bone tissue with fibrous tissue, resulting in irregular bone structure.
Yaxiong Li   +3 more
doaj   +2 more sources

Hearing Loss and Chiari Malformation Type I: A Scoping Review [PDF]

open access: yesDiseases
Background/Objectives: Chiari malformation (CM) type I is an uncommon condition that can be associated with a variety of neurological and otoneurological symptoms, including sensorineural hearing loss.
Andrea Migliorelli   +6 more
doaj   +2 more sources

Prenatal diagnosis of non-typical Chiari malformation type I associated with de novo Nuclear Factor I A gene mutation: a case report [PDF]

open access: yesJournal of Medical Case Reports
Background Chiari malformation is one of the most common Central nervous system (CNS) abnormalities that can be detected in routine fetal scanning. Chiari malformation type I (CMI) is a congenital defect characterized by a displacement of the cerebellar ...
Xuan-Hong Tomai   +4 more
doaj   +2 more sources

Treatment emergent obstructive sleep apnea after Chiari surgery: A case report [PDF]

open access: yesSleep Science, 2020
Patients with Chiari type I malformation may also present with sleep disordered breathing mainly central sleep apnea. Here, we report a patient with Chiari I malformation referred to our clinic because of snoring and sleep ...
Hamed Amirifard   +2 more
doaj   +1 more source

Various manifestation of Chiari I malformation in children and improvement after surgery

open access: yesJournal of Integrative Neuroscience, 2022
Introduction: Chiari I malformation is defined as caudal displacement of the cerebellar tonsils into the foramen magnum. The most commonly associated finding is cervical syringomyelia.
Janez Ravnik   +2 more
doaj   +1 more source

Chiari type I malformation, syncope, headache, hypoglycemia and hepatic steatosis in an 8-year old girl: a causal association?

open access: yesPediatric Reports, 2010
Chiari type I malformation (CMI) is a congenital hindbrain anomaly characterized by downward displacement of the cerebellar tonsils through the foramen magnum.
Alberto Spalice   +5 more
doaj   +1 more source

Chiari Type I Malformation

open access: yesPediatric Neurology Briefs, 1988
A 13-year-old girl with post-traumatic cerebellar ataxia, transient upper extremity weakness, and lower cranial nerve dysfunction was found to have a Type I Chiari malformation on MRI at the Depts of Neurosurgery and Neurology, San Francisco General ...
J Gordon Millichap
doaj   +1 more source

Unusual case of persistent primitive hypoglossal artery with anterior choroidal artery aneurysm in Chiari type I malformation

open access: yesIndian Journal of Radiology and Imaging, 2020
Persistent primitive hypoglossal artery (PPHA) is a rare form of persistent embryonic carotid-basilar anastomosis. We present an unusual case of PPHA and an anterior choroidal artery (AChoA) aneurysm associated with Chiari type I malformation.
Shinya Haryu   +2 more
doaj   +1 more source

Selected Problems of the Patient after the Peak-occipital Decompression Surgery Treatment in the Course of the Chiari type I Malformation

open access: yesPielęgniarstwo Neurologiczne i Neurochirurgiczne, 2018
Introduction. The Chiari type I Malformation is a malformation of the hindbrain and skull. It refers to moving down the tonsils of the cerebellum through a large opening to the upper part of the spinal canal. Case Report.
Beata Haor   +5 more
doaj   +1 more source

Home - About - Disclaimer - Privacy