Results 181 to 190 of about 18,979 (223)
Some of the next articles are maybe not open access.
Journal of Neurosurgery, 1970
✓ In 25 Egyptian patients 2 to 18 years of age, craniosynostosis was studied clinically, radiologically, and biochemically. Oxycephaly was the most common manifestation, but single suture synostosis occurred occasionally. Increased intracranial pressure was marked (76%), clinically, radiologically, and at operation.
H, el-Sherif +3 more
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✓ In 25 Egyptian patients 2 to 18 years of age, craniosynostosis was studied clinically, radiologically, and biochemically. Oxycephaly was the most common manifestation, but single suture synostosis occurred occasionally. Increased intracranial pressure was marked (76%), clinically, radiologically, and at operation.
H, el-Sherif +3 more
openaire +2 more sources
Strabismus in Craniosynostosis
Journal of Pediatric Ophthalmology & Strabismus, 2013Strabismus is common in craniosynostosis, with rates from 39% to 90.9% in Crouzon, Apert, Pfeiffer, and Saethre-Chotzen syndromes. This article reviews the epidemiology of strabismus in these disorders and discusses competing theories of the mechanism, including absent muscles, excyclorotation of muscles, and instability of muscle pulleys.
Jamie B, Rosenberg +2 more
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Hydrocephalus in craniosynostosis
Child's Nervous System, 1988Routine CT scanning in 221 patients with craniosynostosis revealed ventricular dilation in 40. In 5 hydrocephalus was obviously unrelated to the craniostenosis. The remaining 35 cases were associated almost exclusively with syndromic craniosynostosis. Ventricular dilation was mild in 22, moderate in 9, and marked in 4 patients.
H, Collmann +3 more
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Genetic perspectives on craniosynostosis and syndromes with craniosynostosis
Journal of Neurosurgery, 1977✓ Thirty-seven syndromes in which craniosynostosis is a feature are presented in tabular form, allowing the clinician to rapidly identify a given syndrome and gain immediate access to the pertinent literature. A plea is made to delineate unknown genesis syndromes with craniosynostosis as rapidly as possible.
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The Journal of craniofacial surgery (Print), 2020
BACKGROUND Both open cranial vault remodeling (CVR) and endoscopic suturectomy are effective in treating the anatomical deformity of craniosynostosis. While parents are increasingly knowledgeable about these 2 treatment options, information regarding the
Alyson A. Melin +7 more
semanticscholar +1 more source
BACKGROUND Both open cranial vault remodeling (CVR) and endoscopic suturectomy are effective in treating the anatomical deformity of craniosynostosis. While parents are increasingly knowledgeable about these 2 treatment options, information regarding the
Alyson A. Melin +7 more
semanticscholar +1 more source
Oral and Maxillofacial Surgery Clinics of North America, 2020
This article provides an overview of epidemiology, genetics, and common orofacial features of those with craniosynostosis. Patients with craniosynostosis require several surgical procedures along with continuum of care.
Shayna Azoulay-Avinoam +5 more
semanticscholar +1 more source
This article provides an overview of epidemiology, genetics, and common orofacial features of those with craniosynostosis. Patients with craniosynostosis require several surgical procedures along with continuum of care.
Shayna Azoulay-Avinoam +5 more
semanticscholar +1 more source
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
openaire +2 more sources
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 ...
openaire +2 more sources
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
openaire +2 more sources
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
openaire +2 more sources