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Crouzon syndrome: An unwanted family heirloom
TNOA Journal of Ophthalmic Science and ResearchCraniosynostoses are syndromes characterized by premature fusion of sutures of the skull and Crouzon syndrome is the most common of the craniosynostosis syndromes. Early fusion of sutures causes craniofacial anomalies.
Neeharika P Shah, Omkar N Gadre
doaj +1 more source
Acta Cirúrgica Brasileira, 2010 PURPOSE: To verify if uterine cerclage can induce craniosynostosis or any cranial deformity in new born Wistar rats. METHODS: One pregnant female Wistar rat underwent laparotomy on day 18 of gestation and the uterus cervix was closed with a 3-0 nylon ...
Cassio Eduardo Raposo-Amaral +5 more
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Diagnosis and treatment of craniosynostosis: Vilnius team experience
Acta Medica Lituanica, 2015 Background. The aim of the study was to review the methods of diagnosis of craniosynostosis and to analyze Vilnius (Lithuania) team experience of surgical treatment, surgical methods, aspects of anesthesia for patients with craniosynostosis and to ...
Linas Zaleckas +6 more
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The First Korean Case of Beare-Stevenson Syndrome with a Tyr375Cys Mutation in the Fibroblast Growth Factor Receptor 2 Gene [PDF]
, 2007 Here we report the first case of a Korean infant with a cloverleaf-shaped craniosynostosis, in which the diagnosis of Beare-Stevenson syndrome was suspected upon observation of the typical morphological features.
Akai +22 more
core +2 more sources
Revista CEFAC, 2008 TEMA: descrever os aspectos fonoaudiológicos de um caso de Síndrome de Crouzon, com idade de 6:4 anos, submetendo-o às avaliações das áreas de fala, linguagem, cognição, sistema estomatognático e audição.
Isabela Gomes +4 more
doaj +1 more source
ISUOG Practice Guidelines: performance of third‐trimester obstetric ultrasound scan
Ultrasound in Obstetrics &Gynecology, Volume 63, Issue 1, Page 131-147, January 2024.
A. Khalil +7 more
wiley +1 more source
Specific inhibition of fibroblast growth factor receptor 1 signaling by a DNA aptamer
Molecular Therapy: Nucleic AcidsImpaired fibroblast growth factor receptor (FGFR) signaling is associated with many human conditions, including growth disorders, degenerative diseases, and cancer.
Vladimira Zlinska +22 more
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Sagittal craniosynostosis combined with ossified cephalhematoma—a tricky and demanding puzzle [PDF]
, 2018 Introduction: Four cases of sagittal synostosis combined with ossified cephalhematoma prompted the authors to present the data and to discuss the implications.
Kaiser, Georges, Oesch, Valérie
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Molecular Analysis of Twist1 and FGF Receptors in a Rabbit Model of Craniosynostosis: Likely Exclusion as the Loci of Origin [PDF]
, 2013 Craniosynostosis is the premature fusion of the cranial vault sutures. We have previously described a colony of rabbits with a heritable pattern of nonsyndromic, coronal suture synostosis; however, the underlying genetic defect remains unknown.
Cooper, Gregory M. +5 more
core +3 more sources
Abnormal mandibular growth and the condylar cartilage [PDF]
, 2017 Deviations in the growth of the mandibular condyle can affect both the functional occlusion and the aesthetic appearance of the face. The reasons for these growth deviations are numerous and often entail complex sequences of malfunction at the cellular ...
Luder, Hans. U. +3 more
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