Results 21 to 30 of about 15,355 (176)

An Infant with Apert Syndrome and Tetralogy of Fallot for Craniosynostosis Correction: Anesthetic Challenges

open access: yesJournal of Neuroanaesthesiology and Critical Care, 2021
Apert syndrome (AS) is an autosomal dominant disorder characterized by craniosynostosis, craniofacial anomalies, and symmetrical syndactyly of hands and feet. Ten percent children with AS can have associated congenital cardiac anomalies.
Karen R. Lionel   +3 more
doaj   +1 more source

Genetics of Craniosynostosis [PDF]

open access: yes, 2007
Craniosynostosis is a defect of the skull caused by early fusion of one or more of the cranial sutures and affects 3 to 5 individuals per 10,000 live births. Craniosynostosis can be divided into two main groups: syndromic and nonsyndromic.
Hoffman, Trevor L   +4 more
core   +1 more source

Holographic model of craniosynostosis for HoloLens [PDF]

open access: yesActa Cirúrgica Brasileira
Purpose: To develop a holographic skull model of a deformity resulting from craniosynostosis for the HoloLens. Methods: The methodology for product creation and prototyping was the design thinking structured with the double diamond.
Mauricio Mitsuru Yoshida   +5 more
doaj   +1 more source

A Radiation-Free Classification Pipeline for Craniosynostosis Using Statistical Shape Modeling

open access: yesDiagnostics, 2022
Background: Craniosynostosis is a condition caused by the premature fusion of skull sutures, leading to irregular growth patterns of the head. Three-dimensional photogrammetry is a radiation-free alternative to the diagnosis using computed tomography ...
Matthias Schaufelberger   +10 more
doaj   +1 more source

Predictive Value of Sonographic Parameters on the Effects of Cranial Molding Helmet Therapy in Infants with Positional Plagiocephaly

open access: yesDiagnostics
Positional plagiocephaly is a deformational cranial flattening frequently treated in pediatric neurosurgical practice. Positional maneuvers and orthotic helmet therapy are preferred therapeutic options for moderate-to-severe forms.
Maria Licci   +6 more
doaj   +1 more source

Anesthetic management of a rare case of craniosynostosis

open access: yesMedical Journal of Dr. D.Y. Patil University, 2015
Craniosynostosis is a condition of premature intrauterine fusion of sutures causing abnormal skull shape, neurological abnormalities and increased intracranial pressure. It can occur as an isolated condition or may be part of a syndrome.
Smita Joshi   +3 more
doaj   +1 more source

Fronto-orbital advancement: Revisited

open access: yesJournal of Cleft Lip Palate and Craniofacial Anomalies, 2015
Introduction: Craniosynostosis is a pathologic condition resulting from the premature fusion of cranial vault sutures, resulting in craniofacial deformities.
Derick Mendonca   +2 more
doaj   +1 more source

Pharmacological exposures may precipitate craniosynostosis through targeted stem cell depletion

open access: yesStem Cell Research, 2019
The Centers for Disease Control and Prevention, National Birth Defects Study suggests that environmental exposures including maternal thyroid diseases, maternal nicotine use, and use of selective serotonin reuptake inhibitors (SSRIs) may exacerbate ...
Emily Durham   +4 more
doaj   +1 more source

How does nonsyndromic craniosynostosis affect on bone width of nasal cavity in children? - Computed tomography study. [PDF]

open access: yesPLoS ONE, 2018
Craniosynostosis is caused by premature fusion of one or more cranial sutures, restricting skull, brain and face growth. Nonsyndromic craniosynostosis could disturb the proportions of face.
Katarzyna Gruszczyńska   +8 more
doaj   +1 more source

Craniosynostosis genetics: The mystery unfolds

open access: yes, 2011
Craniosynsostosis syndromes exhibit considerable phenotypic and genetic heterogeneity. Sagittal synostosis is common form of isolated craniosynostosis. The sutures involved, the shape of the skull and associated malformations give a clue to the specific ...
Panigrahi, Inusha
core   +3 more sources

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