Results 31 to 40 of about 16,386 (222)

CHIARI MALFORMATIONS IN CHILDREN

Slovenska pediatrija, 2020
Background. Chiari malformations represent different clini-cal and radiological clinical entities that share the herniation of the rhomboencephalic structures through the foramen magnum as a common characteristic.
Peter Spazzapan, Jure Guntar, Borut Prestor   +2 more
doaj   +1 more source

Syringomyelia and Craniocervical Junction Abnormalities in Chihuahuas [PDF]

, 2017
Background: Chiari-like malformation (CM) and syringomyelia (SM) are widely reported in Cavalier King Charles Spaniels and Griffon Bruxellois dogs.
Cappello, Carrera, Cerda-Gonzalez, Cerda-Gonzalez, Cerda-Gonzalez, Cerda-Gonzalez, Couturier, Dewey, Driver, Driver, Driver, Fenn, Freeman, Knowler, Marino, Mitchell, Ortinau, Parker, Rusbridge, Rusbridge, Rusbridge, Rusbridge, Rusbridge, Schmidt, Schmidt, Schmidt, Schmidt, Shaw, Thimineur, Thomson   +29 more
core   +1 more source

Prevalence of disorders recorded in Cavalier King Charles Spaniels attending primary-care veterinary practices in England [PDF]

, 2015
Concerns have been raised over breed-related health issues in purebred dogs, but reliable prevalence estimates for disorders within specific breeds are sparse.
Brodbelt, D C, Church, D B, McGreevy, P D, O'Neill, D G, Summers, J F, Thomson, P C   +5 more
core   +3 more sources

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

Pielęgniarstwo 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, Robert Ślusarz, Agnieszka Królikowska, Renata Jabłońska, Mariola Głowacka, Anita Królikowska   +5 more
doaj   +1 more source

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

American 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, Sylvie A. Adams, Zoe S. Katz, Christal G. Delagrammatikas, Kosuke Izumi, Winifred Sigal, Kim Ventarola, Elaine H. Zackai, Julia E. Reid, Grant T. Liu, Jennifer M. Kalish   +10 more
wiley   +1 more source

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

Indian 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, Naoki Shida, Teiji Tominaga   +2 more
doaj   +1 more source

Descriptive Epidemiology From the Myhre Syndrome Foundation Registry: The Value of Self‐Reported Data

American Journal of Medical Genetics Part C: Seminars in Medical Genetics, EarlyView.
ABSTRACT Myhre syndrome is an ultrarare genetic disease characterized by short stature, distinct craniofacial features, cardiovascular and respiratory fibrosis and stenosis, neurodevelopmental delays, autism, intellectual disability, and hearing loss. The natural history of Myhre syndrome is still not fully understood due to a small patient population ...
Mary K. Young, Armelle Pindon, Maggie R. Brand, Kate Wears, Katherine H. Young, Alyssa Mendel, Michael J. Lyons   +6 more
wiley   +1 more source

Surgical Outcome after Posterior Fossa Decompression with and without Duraplasty in Adult Chiari Malformation Type-I

Egyptian Spine Journal, 2016
Background Data: Adult Chiari malformation is a heterogeneous group of conditions, with the underlying commonality of disruption of normal CSF flow through the foramen magnum. Some cases are congenital, but others are acquired.
Tariq Awad, Mohamed Elqazaz
doaj   +1 more source

Chiari I Malformation: Review and Update of Current Treatment Options

Clinical Anatomy, EarlyView.
ABSTRACT The pathophysiology of Chiari malformation type I (CM‐I) is complex, involving structural abnormalities at the craniovertebral junction that result in herniation of the cerebellar tonsils through the foramen magnum. In this study, we aim to present and evaluate current treatment options for CM‐I, with a focus on evidence‐based clinical ...
Jordan J. Lo, Shuhei Shiino, Stephen Z. Shapiro, Brianna L. Hines, Noritaka Komune, Carmine Antonio Donofrio, Filippo Badaloni, Antonio Fioravanti, Joseph Lockwood, C. J. Bui, Aaron S. Dumont, R. Shane Tubbs   +11 more
wiley   +1 more source

Chiari malformations

Radiologic technology, 2009
Chiari malformations can be serious conditions and their diagnosis often confounds clinicians. When patients present with Chiari malformations, they may have no symptoms or a range of symptoms, many of which can be confused with other neurological conditions.
Jeremy Jones, Frank Gaillard, Rohit Sharma   +2 more
openaire   +3 more sources