Results 191 to 200 of about 13,286 (221)
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Strabismus in craniosynostosis
Current Opinion in Ophthalmology, 2006To present peer-reviewed articles related to strabismus in craniosynostosis.Improved neurosurgical treatment has resulted in amblyopia replacing optic atrophy as the main cause of visual impairment in Apert's and Crouzon syndromes. Patients with nonsyndromic craniosynostosis have an increased incidence of significant refractive error and horizontal ...
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Craniosynostosis and hypophosphatasia
Archives de Pédiatrie, 2017Hypophosphatasia (HPP) when diagnosed at a young age may induce premature fusion of one or several cranial sutures, resulting in a craniocerebral disproportion. The main forms of craniosynostosis associated with HPP are loss of the sagittal suture (scaphocephaly), alone or associated with loss of the coronal sutures (oxycephaly) or associated with loss
F, Di Rocco +4 more
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Archives of Disease in Childhood, 2013
A 4-month-old was referred regarding asymmetry of her head. She was born at term by vaginal delivery weighing 2.21 kg. Her weight, length and head circumference were all on the 0.4th centile. Upon review she was achieving her developmental milestones and thriving along the 2nd centile.
Anna, Rodgers, Neil, Hopper
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A 4-month-old was referred regarding asymmetry of her head. She was born at term by vaginal delivery weighing 2.21 kg. Her weight, length and head circumference were all on the 0.4th centile. Upon review she was achieving her developmental milestones and thriving along the 2nd centile.
Anna, Rodgers, Neil, Hopper
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Plastic and Reconstructive Surgery, 2011
Complex craniosynostoses (i.e., multisutural, nonsyndromic) are rare and present unique treatment challenges. The authors sought to assess long-term outcomes, including postsurgical growth and development, to develop evidence-based treatment algorithms.A retrospective review of all patients identified as having multiple sutural synostosis excluding ...
Marcin, Czerwinski +2 more
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Complex craniosynostoses (i.e., multisutural, nonsyndromic) are rare and present unique treatment challenges. The authors sought to assess long-term outcomes, including postsurgical growth and development, to develop evidence-based treatment algorithms.A retrospective review of all patients identified as having multiple sutural synostosis excluding ...
Marcin, Czerwinski +2 more
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Management of Craniosynostosis
Plastic and Reconstructive Surgery, 2003After studying this article, the participant should be able to: 1. Review the etiopathogenesis of craniosynostosis and craniofacial anomalies. 2. Develop a basic understanding of the clinical manifestations and diagnosis of craniofacial anomalies. 3.
Jayesh, Panchal, Venus, Uttchin
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Etiopathogenesis of Craniosynostosis
Neurosurgery Clinics of North America, 1991Craniosynostosis is both etiologically and pathogenetically heterogeneous. Known causes include monogenic and chromosomal disorders, fetal head constraint, teratogens (aminopterin, diphenylhydantoin, retinoic acid, valproic acid), metabolic diseases (hyperthyroidism, rickets, mucopolysaccharidoses, mucolipidoses), hematologic disorders (thalassemias ...
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Management of Craniosynostosis
Facial Plastic Surgery, 2016Many procedures exist for treatment of craniosynostosis. The goal of all surgical interventions is to correct the skull deformities associated with the synostosis and to prevent the sequela of elevated intracranial pressure. Open cranial vault reconstructions address these issues at the time of surgery, but have the potential for increased blood loss ...
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Neonatal Network, 2009
Craniosynostosis is characterized by the fusion of sutures. It presents with an abnormal head shape. This article examines this defect and discusses its embryologic origin. A systemic physical assessment guide serves as a tool to enhance early recognition of this defect. Pictorial examples increase understanding of the defect. A discussion of treatment
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Craniosynostosis is characterized by the fusion of sutures. It presents with an abnormal head shape. This article examines this defect and discusses its embryologic origin. A systemic physical assessment guide serves as a tool to enhance early recognition of this defect. Pictorial examples increase understanding of the defect. A discussion of treatment
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Craniosynostosis as a risk factor
Child's Nervous System, 1993Craniosynostosis is a little known organic factor in sociopathy. This factor should be among those taken into consideration in selecting patients to undergo craniotomy. Among 22,000 skulls of neuropsychiatric patients, there were 100 with premature coronal synostosis, compared with 57 with dolichocephaly.
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