Results 71 to 80 of about 6,054 (170)

Cyclical vomiting syndrome secondary to a Chiari I malformation - a case report [PDF]

, 2017
Background: Cyclical vomiting syndrome is a disorder characterised by recurrent episodes of profuse vomiting. There are no cases in the literature on the management of children with presenting with cyclical vomiting syndrome and a Chiari malformation ...
Campbell, D.I., William L White, Ushewokunze, S., Shungu Ushewokunze, White, W.L., Veejay Bagga, Bagga, V., Anthony R Hart, Hart, A.R., David I Campbell   +9 more
core   +1 more source

Controversies Surrounding Critical‐Size Defects: Influence of Age and Biological Characteristics

Journal of Biomedical Materials Research Part B: Applied Biomaterials, Volume 114, Issue 6, June 2026.
ABSTRACT Critical‐size defects (CSDs) in craniofacial reconstruction refer to osseous gaps that fail to heal spontaneously, increasing the risk of neurological impairment and craniofacial dysmorphology. Despite decades of investigation, controversy still exists surrounding the definition of CSDs, with criteria varying across species, experimental ...
Andrew Nordlund, Hana Shah, Nicholas A. Mirsky, Kashyap K. Tadisina, Arturo J. Rios‐Diaz, Vasudev Vivekanand Nayak, Estevam A. Bonfante, Paulo G. Coelho   +7 more
wiley   +1 more source

Cardiovascular risk factors in Chiari malformation and idiopathic intracranial hypertension

, 2017
Objectives Both Chiari malformation type 1 (CMI, i.e., the idiopathic caudal ectopy of cerebellar tonsils into foramen magnum) and idiopathic intracranial hypertension (IIH) are characterized by reduced intracranial compliance (ICC) due to disturbed ...
Eide, Per Kristian, Pripp, Are Hugo, Frič, Radek   +2 more
core   +1 more source

Chiari type I malformation in children

, 2011
The diagnosis of Chiari type I malformation (CIM) is more and more frequent in clinical practice due to the wide diffusion of magnetic resonance imaging. In many cases, such a diagnosis is made incidentally in asymptomatic patients, as including children
Massimi, Luca, F. Novegno, Novegno, Federica, L. Massimi, C. di Rocco, Di Rocco, Concezio   +5 more
core   +1 more source

Surgical Management of Chiari Malformation Type I in the Pediatric Patients with Syringomyelia and Related to Klippel-Feil Syndrome: A Case Series and Literature Review

Acta Medica Bulgarica
Chiari type I malformation (CM-1) is a birth defect where the back part of the skull does not develop properly, leading to the formation of a small and shallow space at the back of the head.
Encarnacion-Santos D. A., Chmutin G., Anvardzhonovich I. B., Chmutin E., Arstanbekov B., Kurbonov Sh., Bodanova S., Chaurasia B.   +7 more
doaj   +1 more source

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

Acta 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, Jianfeng Liu, Jian Guan, Conghui Li   +3 more
doaj   +1 more source

Adult chiari type I malformation presenting as dysphagia : a case report [PDF]

The authors describe a rare case of Chiari type I malformation presenting as persistent dysphagia. A fifty-eight year-old woman showing a nearly one-year history of swallowing difficulty was transferred to our department for neurological evaluation of ...

core   +1 more source

Arnold Chiari type III malformation. A case report

, 2023
<p><strong>Background</strong></p><p>Arnold-Chiari malformation is a rare disease, which consists of an anatomical alteration of the base of the skull, in which herniation of the cerebellum and brain stem occurs through the ...
William Francisco Rodriguez Buezo M.D., Sinthia Alejandra Acosta Funez M.D   +1 more
core   +1 more source

Hiccups due to Chiari type I malformation. [PDF]

CMAJ, 2023
Matsuura N.
europepmc   +1 more source

Chiari Type I Malformation Caused by Craniometaphyseal Dysplasia

, 2013
Craniometaphyseal dysplasia is a rare genetic condition characterized by progressive thickening of bones in the skull and metaphyseal abnormalities in the long bones.
Sugimoto, Yoshihisa, Tanaka, Masato, Ozaki, Toshifumi, Arataki, Shinya, Tetsunaga, Tomoko, Takigawa, Tomoyuki   +5 more
core   +1 more source