Literature DB >> 19625842

Intellectual outcomes following protocol management in Crouzon, Pfeiffer, and Muenke syndromes.

Walter J Flapper1, Peter J Anderson, Rachel M Roberts, David J David.   

Abstract

Patients with craniosynostosis syndromes are traditionally managed by a dedicated craniofacial unit. Optimal long-term management of these anomalies is unclear, but in the Australian Craniofacial Unit, it involves ongoing care by an integrated multidisciplinary team, following a protocol that commences at birth and continues until the patient reaches skeletal maturity. The Australian Craniofacial Unit has, for the last 35 years, collected a significant series of patients with these conditions who have completed management from birth to maturity.The aim of this study was to review this series of patients and assess the long-term outcomes of protocol management, focusing in particular on psychologic and social aspects.This review demonstrates that these patients can do well in society, and many achieve higher education and find full-time employment. Regular follow-up and comprehensive multidisciplinary management allows for timely identification of any problems and appropriate intervention. This then helps to maximize the overall outcome for these patients.

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Year:  2009        PMID: 19625842     DOI: 10.1097/SCS.0b013e3181acdf9a

Source DB:  PubMed          Journal:  J Craniofac Surg        ISSN: 1049-2275            Impact factor:   1.046


  8 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.  Executive Function and Adaptive Behavior in Muenke Syndrome.

Authors:  Colin M P Yarnell; Yonit A Addissie; Donald W Hadley; Maria J Guillen Sacoto; Nneamaka B Agochukwu; Rachel A Hart; Edythe A Wiggs; Petra Platte; Yvonne Paelecke; Hartmut Collmann; Tilmann Schweitzer; Paul Kruszka; Maximilian Muenke
Journal:  J Pediatr       Date:  2015-05-28       Impact factor: 4.406

3.  Association between craniofacial anomalies, intellectual disability and autism spectrum disorder: Western Australian population-based study.

Authors:  Mohammed Junaid; Linda Slack-Smith; Kingsley Wong; Jenny Bourke; Gareth Baynam; Hanny Calache; Helen Leonard
Journal:  Pediatr Res       Date:  2022-03-29       Impact factor: 3.953

4.  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

5.  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

6.  Health-related problems and quality of life in patients with syndromic and complex craniosynostosis.

Authors:  Tim de Jong; Marianne Maliepaard; Natalja Bannink; Hein Raat; Irene M J Mathijssen
Journal:  Childs Nerv Syst       Date:  2012-01-11       Impact factor: 1.475

Review 7.  Physiological Changes and Clinical Implications of Syndromic Craniosynostosis.

Authors:  Hiroaki Sakamoto; Yasuhiro Matsusaka; Noritsugu Kunihiro; Keisuke Imai
Journal:  J Korean Neurosurg Soc       Date:  2016-05-10

Review 8.  Cranial Neural Crest Cells and Their Role in the Pathogenesis of Craniofacial Anomalies and Coronal Craniosynostosis.

Authors:  Erica M Siismets; Nan E Hatch
Journal:  J Dev Biol       Date:  2020-09-09
  8 in total

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