Literature DB >> 2065493

Apert syndrome. Classification and pathologic anatomy of limb anomalies.

J Upton1.   

Abstract

This article contains a summary and classification of the major abnormalities seen in both upper and lower extremities associated with Apert syndrome. Whereas rationale and results of treatment of the thumb, hand, foot, shoulder, and elbow can be found in specific articles in this issue, detailed analysis of the anatomy found in the wrist and hand is presented in this article.

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Year:  1991        PMID: 2065493

Source DB:  PubMed          Journal:  Clin Plast Surg        ISSN: 0094-1298            Impact factor:   2.017


  13 in total

1.  Guideline for Care of Patients With the Diagnoses of Craniosynostosis: Working Group on Craniosynostosis.

Authors:  Irene M J Mathijssen
Journal:  J Craniofac Surg       Date:  2015-09       Impact factor: 1.046

2.  Eugène Apert and his contributions to plastic surgery.

Authors:  Dennis S Lee; Kevin C Chung
Journal:  Ann Plast Surg       Date:  2010-03       Impact factor: 1.539

3.  Differential effects of FGFR2 mutations on syndactyly and cleft palate in Apert syndrome.

Authors:  S F Slaney; M Oldridge; J A Hurst; G M Moriss-Kay; C M Hall; M D Poole; A O Wilkie
Journal:  Am J Hum Genet       Date:  1996-05       Impact factor: 11.025

4.  MRI characterization of the glenohumeral joint in Apert syndrome.

Authors:  Tami McHugh; Mary Wyers; Erik King
Journal:  Pediatr Radiol       Date:  2007-04-24

5.  Atypical presentation of a newborn with Apert syndrome.

Authors:  B Spruijt; B F M Rijken; K F M Joosten; H H Bredero-Boelhouwer; B Pullens; M H Lequin; E B Wolvius; M L C van Veelen-Vincent; I M J Mathijssen
Journal:  Childs Nerv Syst       Date:  2014-11-30       Impact factor: 1.475

6.  De novo alu-element insertions in FGFR2 identify a distinct pathological basis for Apert syndrome.

Authors:  M Oldridge; E H Zackai; D M McDonald-McGinn; S Iseki; G M Morriss-Kay; S R Twigg; D Johnson; S A Wall; W Jiang; C Theda; E W Jabs; A O Wilkie
Journal:  Am J Hum Genet       Date:  1999-02       Impact factor: 11.025

7.  Analysis of phenotypic features and FGFR2 mutations in Apert syndrome.

Authors:  W J Park; C Theda; N E Maestri; G A Meyers; J S Fryburg; C Dufresne; M M Cohen; E W Jabs
Journal:  Am J Hum Genet       Date:  1995-08       Impact factor: 11.025

8.  Unilateral Coronal Craniosynostosis in an Apert-Like Patient.

Authors:  Navid Pourtaheri; Derek Z Wang; Robert P Lesko; Christopher M Bonfield; Peter Taub; Anand R Kumar
Journal:  Plast Surg (Oakv)       Date:  2018-10-03       Impact factor: 0.947

9.  Infrared venography of the hand in Apert syndrome.

Authors:  Soh Nishimoto; Kenji Fukuda; Toshihiro Fujiwara; Masato Kinoshita; Kenichiro Kawai; Masao Kakibuchi
Journal:  Indian J Plast Surg       Date:  2013-09

10.  Deformed Skull Morphology Is Caused by the Combined Effects of the Maldevelopment of Calvarias, Cranial Base and Brain in FGFR2-P253R Mice Mimicking Human Apert Syndrome.

Authors:  Fengtao Luo; Yangli Xie; Wei Xu; Junlan Huang; Siru Zhou; Zuqiang Wang; Xiaoqing Luo; Mi Liu; Lin Chen; Xiaolan Du
Journal:  Int J Biol Sci       Date:  2017-01-01       Impact factor: 6.580

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