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Acrocephalosyndactylia (Latest Articles)
Latest indexed articles for 'Acrocephalosyndactylia'
Articles 141 to 150 of 200:
Le Fort III distraction osteogenesis in syndromal craniosynostosis.
30 Dec 2005 
Midface distraction osteogenesis has become a valuable technique. Although outcome data are available from several craniofacial centers, information regarding perioperative and immediate postoperative course is scarce. This report describes seven ...
rec_pub_16432404-le-fort-iii-distraction-osteogenesis-syndromal-craniosynostosis.htm
Cranial vault distraction: its illusionary effect and limitation.
30 Dec 2005 BACKGROUND: Distraction osteogenesis has some advantages, such as less hazardous complications, less scarring, and fewer bone defects. However, it has not been fully accepted yet because of a unidirectional expansion along the distraction device. ...
rec_pub_16404266-cranial-vault-distraction-illusionary-effect-limitation.htm
Combined push-pull distraction for correction of syndromic midfacial hypoplasia.
30 Dec 2005 PURPOSE: Gradual midfacial advancement, applying the principle of distraction osteogenesis, reduces the restriction of the soft tissues and results in bony consolidation without need for grafting. The midface can be distracted by either pushing it ...
rec_pub_16360853-combined-push-pull-distraction-correction-syndromic-midfacial.htm
Metopic suture in fetuses with Apert syndrome at 22-27 weeks of gestation.
30 Dec 2005 OBJECTIVES: To examine the possible association of skull deformity and the development of the cranial sutures in fetuses with Apert syndrome. METHODS: Three-dimensional (3D) ultrasound was used to examine the metopic and coronal sutures in seven ...
rec_pub_16317802-metopic-suture-fetuses-apert-syndrome-22-27-weeks-gestation.htm
30 Dec 2005 
The Saethre-Chotzen syndrome (SCS) is an autosomal dominant craniosynostosis syndrome with uni- or bilateral coronal synostosis and mild limb deformities. It is caused by loss-of-function mutations of the TWIST 1 gene. In an attempt to delineate ...
rec_pub_16251895-saethre-chotzen-syndrome-caused-twist-1-gene-mutations-functional.htm
Inhibition or activation of Apert syndrome FGFR2 (S252W) signaling by specific glycosaminoglycans.
20 Dec 2005 Most Apert syndrome patients harbor a single amino acid mutation (S252W) in fibroblast growth factor (FGF) receptor 2 (FGFR2), which leads to abnormal FGF/FGFR2 signaling. Here we show that specific combinations of FGFs and glycosaminoglycans ...
rec_pub_16373332-inhibition-activation-apert-syndrome-fgfr2-s252w-signaling-specific.htm
Apert syndrome: factors involved in the cognitive development.
13 Dec 2005 Apert syndrome is characterized by craniosynostosis, symmetric syndactyly and other systemic malformations, with mental retardation usually present. The objective of this study was to correlate brain malformations and timing for surgery with ...
rec_pub_16400413-apert-syndrome-factors-involved-cognitive-development.htm
Saethre-Chotzen syndrome: a case report.
29 Nov 2005 
rec_pub_16503569-saethre-chotzen-syndrome-case-report.htm
The Wnt-inducible transcription factor Twist1 inhibits chondrogenesis.
15 Nov 2005 Wnt signaling is essential for many developmental processes, including skeletogenesis. To investigate the effects of Wnt signaling during skeletogenesis we studied the effects of Wnt on cultured chondrocytic cells and differentiating limb-bud ...
rec_pub_16293629-the-wnt-inducible-transcription-factor-twist1-inhibits-chondrogenesis.htm
Successful acne management in Apert syndrome twins.
30 Oct 2005 Apert syndrome, or acrocephalosyndactyly, is characterized by craniosynostosis and early epiphyseal closure resulting in various deformities of the skull, hands, and feet. Typically a sporadic condition, autosomal dominant inheritance with complete ...
rec_pub_16354263-successful-acne-management-apert-syndrome-twins.htm
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