Results 21 to 30 of about 6,054 (170)

Anestesia pada Tindakan Dekompresi Foramen Magnum pada Pasien dengan Malformasi Arnold Chiari

open access: yesJurnal Neuroanestesi Indonesia, 2013
Malformasi Arnold Chiari tipe 1 adalah pergeseran tonsil serebellum kearah kaudal kanalis spinalis tulang belakang servikal melalui foramen magnum. Siringomielia adalah gangguan degeneratif progresif yang ditandai dengan amiotropi brakhial dan kehilangan
Nazaruddin Umar   +2 more
doaj   +1 more source

Acquired Chiari malformation type I associated with a supratentorial fistulous arteriovenous malformation: a case report

open access: yes, 2017
A case of acquired Chiari malformation type I with frontal fistulous arteriovenous malformation (AVM) is presented, and the pathophysiology is discussed. The tonsillar herniation and hydrocephalus both resolved after AVM was excised.
杜永光;郭夢菲;李崇維   +1 more
core   +1 more source

The significance of occipitocervical dura angulation in selection of surgery procedures for Chiari malformation type I

open access: yesJournal of Neurorestoratology, 2019
At present, the common surgical procedures for the Chiari malformation type I are comprised of posterior fossa decompression, duraplasty and tonsillectomy. Some neurosurgeons prefer these so called minimally invasive surgeries.
Bo Xiu, Rui Zhang
doaj   +1 more source

Malformations of the craniocervical junction: Casamassima-morton-nance syndrome and type I Chiari malformation

open access: yesInterdisciplinary Neurosurgery, 2021
Introduction: Casamassima-Morton-Nance syndrome (CMNS) is a rare pathology with few reports in the literature. CMNS, Jarcho-Levine syndrome and the Lavy-Moseley syndrome must be considered among the differential diagnoses on those patients with vertebral
Juan Esteban Muñoz-Montoya   +5 more
doaj   +1 more source

Postoperative epidural hematoma contributes to delayed upper cord tethering after decompression of Chiari malformation type I.

open access: yes, 2014
Symptomatic arachnoiditis after posterior fossa surgical procedures such as decompression of Chiari malformation is a possible complication. Clinical presentation is generally insidious and delayed by months or years. It causes disturbances in the normal
Márquez-Rivas, Francisco Javier   +2 more
core   +1 more source

Incidental Detection of Arnold Chiari – I Malformation on MRI in a Case of Neck Pain [PDF]

open access: yesInternational Journal of Anatomy Radiology and Surgery, 2016
Chiari malformations are spectrum of congenital hindbrain abnormalities. With advancing use of MR imaging, Chiari malformation is discovered with increasing frequency.
Pokhraj Prakashchandra Suthar   +3 more
doaj   +1 more source

Bony decompression for chiari malformation type I: Long-term follow-up

open access: yes, 2019
Background: Several surgical techniques are used for the management of Chiari malformation type I (CM-I). Bony posterior fossa decompression is considered a good option in children, though with a higher risk of requiring reoperation.
Tamburrini, Gianpiero   +8 more
core   +1 more source

Phenotype Expansion of Malan Syndrome: New Cases and a Review of the Literature

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Malan syndrome is an ultra‐rare overgrowth syndrome caused by pathogenic variants or deletions in nuclear factor one X (NFIX) located at 19p13.2. Here, we report a comprehensive literature review and phenotyping of known patients with Malan syndrome and present a novel cohort of eight patients.
Alex F. Nisbet   +10 more
wiley   +1 more source

Acquired Chiari type I malformation: a late and misunderstood supratentorial over-drainage complication

open access: yes, 2023
Purpose: Acquired Chiari I malformation is an uncommon but possible late complication of supratentorial shunting in children. This condition can be caused by an abnormal thickening of the cranial vault and consequent reduction of the posterior cranial ...
Furlanis G. M.   +6 more
core   +1 more source

The Homozygous p.(Arg215Ter) Variant in XRCC2 Is Associated With Atypical Fanconi Anemia Without Major Hematological Abnormalities in Childhood

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Fanconi Anemia (FA) is the most frequent inherited bone marrow failure syndrome. A role for the XRCC2 gene in FA was suspected in 2012 and confirmed in 2016, but only two affected individuals have been described thus far, and no long‐term follow‐up is available.
Sabina Cenciarelli   +11 more
wiley   +1 more source

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