Acrocephalosyndactylia (Latest Articles)

Latest indexed articles for 'Acrocephalosyndactylia'

Articles 41 to 50 of 200:

[Syndactyly]

20 Aug 2008 Syndactyly is one of the most common congenital anomalies of the hand. It can be isolated or associated with systemic syndromes. Surgical treatment is performed between the ages of six and 18 months depending on the type and extent of the ...
rec_pub_18842447-syndactyly.htm

[The Apert's syndrome hand: therapeutic management]

18 Aug 2008 Apert's syndrome is the most common among acrocephalosyndactylies with complex malformations of the hands. Treatment of the Apert hand is complex and numerous procedures are required. The aim of this study is to propose a strategy for hand ...
rec_pub_18842437-the-apert-s-syndrome-hand-therapeutic-management.htm

A germ-line-selective advantage rather than an increased mutation rate can explain some unexpectedly common human disease mutations.

14 Jul 2008 Two nucleotide substitutions in the human FGFR2 gene (C755G or C758G) are responsible for virtually all sporadic cases of Apert syndrome. This condition is 100-1,000 times more common than genomic mutation frequency data predict. Here, we report on ...
rec_pub_18632557-a-germ-line-selective-advantage-increased-mutation-rate-explain.htm

Apert syndrome: review and report a case.

29 Jun 2008
rec_pub_18853000-apert-syndrome-review-report-case.htm

Brachycephaly and syndactyly: Apert's syndrome.

29 Jun 2008
rec_pub_18797073-brachycephaly-syndactyly-apert-s-syndrome.htm

Blindness as a complication of monobloc frontofacial advancement with distraction.

29 Jun 2008 The monobloc frontofacial osteotomy provides aesthetic and functional improvement in the treatment of various craniofacial deformities. This procedure, through highly complex, has had some significant associated complication, such as cerebrospinal ...
rec_pub_18650754-blindness-complication-monobloc-frontofacial-advancement-distraction.htm

Axillary osmidrosis in Apert syndrome: management with an arthroscopic shaver technique.

29 Jun 2008 Apert syndrome is a congenital condition characterized by craniosynostosis, syndactyly, and maxillary hypoplasia. Previous authors have outlined the management of craniofacial and extremity anomalies associated with this syndrome; however, there is ...
rec_pub_18650746-axillary-osmidrosis-apert-syndrome-management-arthroscopic-shaver.htm

Three-dimensional image analysis of facial skeletal changes after monobloc and bipartition distraction.

29 Jun 2008 BACKGROUND: Both monobloc and facial bipartition distraction are important tools for correcting functional and aesthetic problems in patients with syndromic craniosynostosis. Three-dimensional computed tomographic reconstructions have become ...
rec_pub_18594409-three-dimensional-image-analysis-facial-skeletal-changes-monobloc.htm

Pfeiffer syndrome with neonatal death secondary to tracheal obstruction owing to the FGFR2 Glu565Ala mutation.

29 Jun 2008
rec_pub_18541976-pfeiffer-syndrome-neonatal-death-secondary-tracheal-obstruction-owing.htm

A rare case of Pfeiffer's syndrome.

29 Apr 2008
rec_pub_18604693-a-rare-case-pfeiffer-s-syndrome.htm

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