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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]
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]
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
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
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
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
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
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]
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
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

