Results 1 to 10 of about 833 (169)

Platybasia in 22q11.2 Deletion Syndrome Is Not Correlated with Speech Resonance [PDF]

open access: yesArchives of Plastic Surgery, 2014
Background An abnormally obtuse cranial base angle, also known as platybasia, is a common finding in patients with 22q11.2 deletion syndrome (22q11DS).
Nicole E Spruijt   +2 more
doaj   +6 more sources

Basilar invagination in osteogenesis imperfecta—Case report [PDF]

open access: yesRadiology Case Reports
Osteogenesis imperfecta (OI) is a genetic disorder characterized by defective type I collagen synthesis, leading to fragile bones and skeletal deformities.
Aviyani Aviyani, Raisa Mahmudah
doaj   +2 more sources

Treatment of Chiari malformations with craniovertebral junction anomalies: Where do we stand today? [PDF]

open access: yesWorld Neurosurgery: X, 2023
Background: Chiari malformation type 1 (CM-1) is characterized by cerebellar tonsil herniation through the foramen magnum and can be associated with additional craniovertebral junction anomalies (CVJA).
Sima Vazquez   +8 more
doaj   +2 more sources

The interleukin-11 receptor variant p.W307R results in craniosynostosis in humans [PDF]

open access: yesScientific Reports, 2023
Craniosynostosis is characterized by the premature fusion and ossification of one or more of the sutures of the calvaria, often resulting in abnormal features of the face and the skull.
Ilyas Ahmad   +15 more
doaj   +3 more sources

A rare case of pancraniosynostosis observed in a historical skull from the 19 th century cranial collection named “Królestwo Polskie” (“Polish Kingdom”) [PDF]

open access: yesAnthropological Review, 2021
Rare diseases are a challenge in paleopathological research, mainly due to the ambiguity of skeletal signs, bad preservation state of the material, and lack of the reference material.
Cieślik Agata   +3 more
doaj   +2 more sources

Acquired Chiari Type 1 Malformation Secondary to Paget’s Disease of the Bone: A Case Report [PDF]

open access: yesJournal of Clinical and Diagnostic Research, 2021
Chiari type 1 malformations are characterised by caudal descent of cerebellar tonsil into foramen magnum. Usually it is congenital. Paget’s disease causing acquired chiari type 1 malformation is rare with only five reported cases in the literature.
Srestha Khan   +3 more
doaj   +1 more source

Where does the cranial base flexion take place in humans? [PDF]

open access: yesAnais da Academia Brasileira de Ciências, 2020
The modern human has the most flexed cranial base among all living animals. The flexure allowed a larger cranial volume to accommodate a greater brain. Spheno-occipitalis synchondrosis (SOS) has been largely responsible for cranial base flexion, between ...
RICARDO V. BOTELHO   +2 more
doaj   +1 more source

Influence of the Severity of Osteogenesis Imperfecta on Cranial Measurements

open access: yesChildren, 2023
Osteogenesis Imperfecta (OI) is a disease that causes bone fragility and deformities, affecting both the cranial base and the craniocervical junction, and may lead to other neurological disorders.
Manuel Joaquín De Nova-García   +2 more
doaj   +1 more source

Radiological Imaging Findings of Basilar Invagination

open access: yesVan Tıp Dergisi, 2020
INTRODUCTION: To evaluate craniometric measurements and accompanying additional pathologies in cases with basilar invagination on radiological imaging.
Murat Beyhan   +2 more
doaj   +1 more source

Impacted cisterna magna without syringomyelia associated or not with basilar impression and/or Chiari malformation

open access: yesBrazilian Neurosurgery, 2013
Objective: The objective of this paper is to analyze the surgical treatment of impacted cisterna magna without syringomyelia (SM) associated or not with basilar impression (BI) and/or Chiari malformation (CM).
José Alberto Gonçalves da Silva   +2 more
doaj   +1 more source

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