Results 41 to 50 of about 3,158 (217)
Treatment of pressure gun fractures and release in the wild of a caracara (Caracara plancus)
Abstract This report aims to describe the treatment progression of a free‐living southern crested caracara (Caracara plancus plancus) with gunshot‐related fractures. Radiographic examination revealed a comminuted fracture in the mid‐diaphysis of the humerus with displaced fragments, a comminuted fracture of the proximal third of the radius shaft, and ...
Guilherme Rech Cassanego +4 more
wiley +1 more source
Crouzon Syndrome: a Comprehensive Review
Crouzon syndrome is a rare genetic disorder with autosomal dominant inheritance. The underlying pathological process is premature synostosis of the cranial sutures with subsequent phenotypic alterations of the affected person.
Kyprianou Chrystalla +1 more
doaj +1 more source
Cranial neural crest cell contribution to craniofacial formation, pathology, and future directions in tissue engineering [PDF]
Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/108634/1/bdrc21075 ...
Achilleos +51 more
core +1 more source
Genetic and Molecular Determinants of Familial Transmission of Skeletal Malocclusions
ABSTRACT Families studies conducted in different ethnic populations worldwide have helped elucidate the molecular and genetic factors involved in the development of skeletal class III malocclusion. Therefore, the aim of this study is to provide an updated summary.
Alexandra Dehesa‐Santos +3 more
wiley +1 more source
Background:. Premature fusion of the sagittal (midline) suture between 2 parietal bones is the most common form of craniosynostosis. Surgical correction is mandated to improve head shape and to decrease the risk of raised intracranial pressure.
William X.Z. Liaw, MD +7 more
doaj +1 more source
ABSTRACT Diamond Blackfan anemia (DBA) is an autosomal dominant disorder with a heterogeneous clinical presentation which may include macrocytic anemia typically presenting in the first year of life, growth retardation, and congenital malformations in 30%–50% of patients.
Lisa M. Karger +4 more
wiley +1 more source
Crouzon's syndrome: A case report and review
Crouzon's syndrome is a rare genetic disorder characterized by distinctive craniofacial malformations. The disease is characterized by premature synostosis of coronal and sagittal sutures which begins in the 1st year of life.
Candice Jacinta Antao +3 more
doaj +1 more source
Three-Dimensional Handheld Scanning to Quantify Head-Shape Changes in Spring-Assisted Surgery for Sagittal Craniosynostosis [PDF]
Three-dimensional (3D) imaging is an important tool for diagnostics, surgical planning, and evaluation of surgical outcomes in craniofacial procedures. Gold standard for acquiring 3D imaging is computed tomography that entails ionizing radiations and, in
Angullia, F +8 more
core +1 more source
Rekonstruktive und plastische Operationen in der Kinderneurochirurgie
Cranial and spinal congenital disorders are the main reason for operative therapy in pediatric patients. Other indications are tumour surgery and trauma.
Ludwig, H. C., Bock, H. C.
doaj +1 more source

