Literature DB >> 1519659

Upper and lower airway compromise in the Apert syndrome.

M M Cohen1, S Kreiborg.   

Abstract

Both upper and lower airway compromise may be responsible for early death in some patients with the Apert syndrome. We report on two and review six cases with complete or partial cartilage sleeve abnormalities of the trachea. Possible mechanisms include tracheal stenosis and/or lack of tracheal distensibility which may result in respiratory inefficiency, inability to clear secretions, and/or increased liability to surface injury from tracheal suctioning. Upper airway compromise, consisting of obstructive sleep apnea and cor pulmonale, may result from reduced nasopharyngeal and oropharyngeal dimensions in the Apert craniofacial configuration.

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Year:  1992        PMID: 1519659     DOI: 10.1002/ajmg.1320440121

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  14 in total

1.  Mesodermal expression of Fgfr2S252W is necessary and sufficient to induce craniosynostosis in a mouse model of Apert syndrome.

Authors:  Greg Holmes; Claudio Basilico
Journal:  Dev Biol       Date:  2012-06-01       Impact factor: 3.582

Review 2.  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

Review 3.  Complex craniosynostoses: a review of the prominent clinical features and the related management strategies.

Authors:  G Tamburrini; M Caldarelli; L Massimi; G Gasparini; S Pelo; C Di Rocco
Journal:  Childs Nerv Syst       Date:  2012-08-08       Impact factor: 1.475

4.  Pediatric sleep apnea and craniofacial anomalies: a population-based case-control study.

Authors:  Derek J Lam; Christine C Jensen; Beth A Mueller; Jacqueline R Starr; Michael L Cunningham; Edward M Weaver
Journal:  Laryngoscope       Date:  2010-10       Impact factor: 3.325

Review 5.  Airway management in neuroanaesthesia.

Authors:  B F Spiekermann; D J Stone; D L Bogdonoff; T A Yemen
Journal:  Can J Anaesth       Date:  1996-08       Impact factor: 5.063

6.  Further analysis of the Crouzon mouse: effects of the FGFR2(C342Y) mutation are cranial bone-dependent.

Authors:  Jin Liu; Hwa Kyung Nam; Estee Wang; Nan E Hatch
Journal:  Calcif Tissue Int       Date:  2013-01-29       Impact factor: 4.333

7.  Tissue-nonspecific alkaline phosphatase deficiency causes abnormal craniofacial bone development in the Alpl(-/-) mouse model of infantile hypophosphatasia.

Authors:  Jin Liu; Hwa Kyung Nam; Cassie Campbell; Kellen Cristina da Silva Gasque; José Luis Millán; Nan E Hatch
Journal:  Bone       Date:  2014-07-09       Impact factor: 4.398

8.  Fibroblast growth factor 10 plays a causative role in the tracheal cartilage defects in a mouse model of Apert syndrome.

Authors:  Caterina Tiozzo; Stijn De Langhe; Gianni Carraro; Denise Al Alam; Andre Nagy; Clarence Wigfall; Mohammad K Hajihosseini; David Warburton; Parviz Minoo; Saverio Bellusci
Journal:  Pediatr Res       Date:  2009-10       Impact factor: 3.756

9.  Midface and upper airway dysgenesis in FGFR2-related craniosynostosis involves multiple tissue-specific and cell cycle effects.

Authors:  Greg Holmes; Courtney O'Rourke; Susan M Motch Perrine; Na Lu; Harm van Bakel; Joan T Richtsmeier; Ethylin Wang Jabs
Journal:  Development       Date:  2018-10-05       Impact factor: 6.868

10.  Tracheal cartilaginous sleeves in children with syndromic craniosynostosis.

Authors:  Tara L Wenger; John Dahl; Elizabeth J Bhoj; Anna Rosen; Donna McDonald-McGinn; Elaine Zackai; Ian Jacobs; Carrie L Heike; Anne Hing; Avni Santani; Andrew F Inglis; Kathleen C Y Sie; Michael Cunningham; Jonathan Perkins
Journal:  Genet Med       Date:  2016-05-26       Impact factor: 8.822

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