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Acrocephalosyndactylia (Latest Articles)
Latest indexed articles for 'Acrocephalosyndactylia'
Articles 11 to 20 of 200:
Ocular advancement in monobloc distraction.
29 Apr 2009 
BACKGROUND: Monobloc distraction has been demonstrated to be an efficacious, safe, and stable method of providing functional and aesthetic improvement in children with syndromic craniosynostosis. Although the movement of bony structures following ...
rec_pub_19407630-ocular-advancement-monobloc-distraction.htm
Pfeiffer syndrome: a treatment evaluation.
29 Apr 2009 BACKGROUND: Pfeiffer syndrome is rarely encountered, even at major craniofacial centers. Published reports indicate high mortality rates (25 to 85 percent) for severely affected subtypes. The authors reviewed their surgically treated patients to ...
rec_pub_19407629-pfeiffer-syndrome-treatment-evaluation.htm
Cloverleaf skulls: etiologic heterogeneity and pathogenetic variability.
27 Feb 2009 Cloverleaf skulls (Kleeblattschädel-Syndromen, trilobular skulls) have different modes of development (pathogenetic variability). Synostosis may involve various sutures in different types of cloverleaf skulls. Their facial features, radiographic ...
rec_pub_19293681-cloverleaf-skulls-etiologic-heterogeneity-pathogenetic-variability.htm
The evaluation of bony union after frontofacial distraction.
27 Feb 2009 Frontofacial advancement by distraction osteogenesis using the rigid external distraction device has become an accepted treatment for the deformity associated with craniofacial dysostoses (e.g., Crouzon, Apert, and Pfeiffer syndromes). The technical ...
rec_pub_19258910-the-evaluation-bony-union-frontofacial-distraction.htm
Pyrexia after transcranial surgery for Pfeiffer syndrome.
27 Feb 2009 BACKGROUND: Previously, we have reported the pattern of temperature increase after transcranial surgery for nonsyndromic craniosynostosis. It was found that pyrexia had a bimodal distribution during the first 48 hours after surgery. AIM: The aims of ...
rec_pub_19242364-pyrexia-transcranial-surgery-pfeiffer-syndrome.htm
27 Feb 2009 
rec_pub_19025794-germline-mutation-fgfr3-gene-twist1-negative-family-saethre-chotzen.htm
BaS analysis: a new cephalometric study for craniofacial malformations.
25 Feb 2009 OBJECT: Patients submitted to surgical advancement of the upper and middle facial third might have a relapse of the skeletal retraction after the removal of the distractor devices. Clinical signs related to this process are usually represented by ...
rec_pub_19247673-bas-analysis-new-cephalometric-study-craniofacial-malformations.htm
Three-dimensional features of Pfeiffer syndrome.
18 Feb 2009
rec_pub_19232609-three-dimensional-features-pfeiffer-syndrome.htm
30 Jan 2009 Apert syndrome (AS) is a severe congenital disease caused by mutations in fibroblast growth factor receptor-2 (FGFR2), and characterised by craniofacial, limb, visceral, and neural abnormalities. AS-type FGFR2 molecules exert a gain-of-function ...
rec_pub_18773495-evidence-fgf10-contributes-skeletal-visceral-defects-apert-syndrome.htm
Comparison of periodontal parameters in individuals with syndromic craniosynostosis.
30 Dec 2008 
Craniosynostosis syndromes are characterized by premature closure of one or more cranial sutures, associated with other malformations, the most frequent of which are the Crouzon and Apert syndromes. Few studies in the literature have addressed the ...
rec_pub_19148400-comparison-periodontal-parameters-individuals-syndromic.htm
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