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Treacher Collins-Franceschetti Syndrome

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Modern Microtia Reconstruction

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Abstract

The most typical feature of Treacher Collins-Franceschetti syndrome is the antimongoloid slant of the palpebral fissures. This is due to absence or hypoplasia of the zygomatic-malar buttress and ectropion of the lower lid. Reconstruction with cranial bone grafts, upper lid flaps, and lateral canthopexy consents progressive normalization of facial features.

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Author information

Authors and Affiliations

  1. Bambino Gesu Hospital, Plastic Surgery Unit, Rome, Italy

    Patricia Cecchi

  2. Clinique Chateaux de la Maye, Paris, France

    Darina Krastinova

Authors
  1. Patricia Cecchi
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  2. Darina Krastinova
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Editor information

Editors and Affiliations

  1. Keck School of Medicine, University of Souther California, Los Angeles, CA, USA

    John F. Reinisch

  2. Plastic and Reconstructive Surgery, Cedars-Sinai Medical Center, Los Angeles, CA, USA

    Youssef Tahiri

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Cecchi, P., Krastinova, D. (2019). Treacher Collins-Franceschetti Syndrome. In: Reinisch, J., Tahiri, Y. (eds) Modern Microtia Reconstruction. Springer, Cham. https://doi.org/10.1007/978-3-030-16387-7_15

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  • DOI: https://doi.org/10.1007/978-3-030-16387-7_15

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  • Publisher Name: Springer, Cham

  • Print ISBN: 978-3-030-16386-0

  • Online ISBN: 978-3-030-16387-7

  • eBook Packages: MedicineMedicine (R0)

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