Literature DB >> 20216456

Management of craniofacial hyperostosis in Proteus syndrome.

Yoshiaki Sakamoto1, Hideo Nakajima, Kazuo Kishi, Ruka Shimizu, Tatsuo Nakajima.   

Abstract

Proteus syndrome is a rare congenital hamartomatous condition that is characterized by a wide range of malformations, occasionally involving the head and the face. Skin and skeletal developmental malformations are common and may be manifested in significant physical anomalies. In this report, we describe the cases of 2 patients affected by this condition. For one patient, a recurrence occurred 4 years after the elimination of cranial hyperostosis. In the second patient, although we observed macrosomia and peculiar countenance in the context of craniofacial hyperostosis, the patient did not visit a clinic for approximately 50 years before seeking treatment. The management of the craniofacial involvement is described, and a literature overview is presented.

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Year:  2010        PMID: 20216456     DOI: 10.1097/SCS.0b013e3181cfa7f0

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


  4 in total

1.  Phenotype and Surgical Treatment in a Case of Proteus Syndrome With Craniofacial and Oral Findings.

Authors:  Reinhard E Friedrich
Journal:  In Vivo       Date:  2021 May-Jun       Impact factor: 2.155

2.  Proteus syndrome revealing itself after the treatment of a bilateral subdural haematoma.

Authors:  Yassine El Hassani; Benoit Jenny; Brigitte Pittet-Cuenod; Armand Bottani; Paolo Scolozzi; Hulya Ozsahin Ayse; Benédict Rilliet
Journal:  Childs Nerv Syst       Date:  2013-04-05       Impact factor: 1.475

3.  Craniofacial and dental development in Costello syndrome.

Authors:  Alice F Goodwin; Snehlata Oberoi; Maya Landan; Cyril Charles; Jessica C Massie; Cecilia Fairley; Katherine A Rauen; Ophir D Klein
Journal:  Am J Med Genet A       Date:  2014-03-25       Impact factor: 2.802

4.  Potential pitfalls in volume reduction for the treatment of Proteus syndrome.

Authors:  C Tsue; Y Sakamoto; Y Nakajima; K Kishi
Journal:  J Surg Case Rep       Date:  2012-10-01
  4 in total

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