Literature DB >> 2065483

Clinical assessment and multispecialty management of Apert syndrome.

L C Kaplan1.   

Abstract

This article has provided an overview of the medical, surgical, and developmental issues that should be considered in all individuals with the Apert syndrome. This is a multiple-malformation syndrome and, as such, health care must involve attention to multiple systems. In addition to a planned strategy for surgical management, family history must be considered and consultations requested with a geneticist, ophthalmologist, child development specialist, and an otorhinolaryngologist in addition to the "team" members described. Potential complications from airway obstruction include obstructive breathing patterns, apnea, and cor pulmonale; central nervous system abnormalities may not be apparent until neurologic sequelae are manifested. The single most important concept of team care rests not with close proximity of multiple specialists but with the ability of the team to communicate and organize effectively a plan of care for families.

Entities:  

Mesh:

Year:  1991        PMID: 2065483

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


  5 in total

1.  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

2.  Comparison of ultrasound and magnetic resonance imaging in the prenatal diagnosis of Apert syndrome: report of a case.

Authors:  A Giancotti; V D'Ambrosio; A De Filippis; C Aliberti; G Pasquali; S Bernardo; L Manganaro
Journal:  Childs Nerv Syst       Date:  2014-02-25       Impact factor: 1.475

3.  FGFR-associated craniosynostosis syndromes and gastrointestinal defects.

Authors:  Christine E Hibberd; Sarah Bowdin; Yamini Arudchelvan; Christopher R Forrest; Katherine A Brakora; Ralph S Marcucio; Siew-Ging Gong
Journal:  Am J Med Genet A       Date:  2016-08-02       Impact factor: 2.802

4.  Bilateral squamosal suture synostosis: A rare form of isolated craniosynostosis in Crouzon syndrome.

Authors:  Yasmeen K Tandon; Michael Rubin; Mohamed Kahlifa; Gaby Doumit; Lena Naffaa
Journal:  World J Radiol       Date:  2014-07-28

5.  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

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.