Literature DB >> 5938051

Progressive synosteosis in Apert's syndrome (acrocephalosyndactyly), with a description of roentgenographic changes in the feet.

E W Schauerte, P M St-Aubin.   

Abstract

Entities:  

Mesh：

Year:  1966        PMID： 5938051     DOI： 10.2214/ajr.97.1.67

Source DB:  PubMed          Journal:  Am J Roentgenol Radium Ther Nucl Med        ISSN： 0002-9580


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  5 in total

1.  Syndrome designations.

Authors:  M M Cohen
Journal:  J Med Genet       Date:  1976-08       Impact factor: 6.318

Review 2.  Talocalcaneal coalition in Muenke syndrome: report of a patient, review of the literature in FGFR-related craniosynostoses, and consideration of mechanism.

Authors:  Nneamaka B Agochukwu; Benjamin D Solomon; Laurel J Benson; Maximilian Muenke
Journal:  Am J Med Genet A       Date:  2013-02-01       Impact factor: 2.802

Review 3.  Impact of genetics on the diagnosis and clinical management of syndromic craniosynostoses.

Authors:  Nneamaka B Agochukwu; Benjamin D Solomon; Maximilian Muenke
Journal:  Childs Nerv Syst       Date:  2012-08-08       Impact factor: 1.475

4.  Perspectives on Craniosynostosis.

Authors:  M M Cohen
Journal:  West J Med       Date:  1980-06

Review 5.  Is the Apert foot an overlooked aspect of this rare genetic disease? Clinical findings and treatment options for foot deformities in Apert syndrome.

Authors:  Alexandra Stauffer; Sebastian Farr
Journal:  BMC Musculoskelet Disord       Date:  2020-11-28       Impact factor: 2.362
  5 in total

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