IDEAS home Printed from https://ideas.repec.org/a/epw/ejmed0/v4y2022i1id41227.html

Congenital Lower Lip Pits: A Familial Case of Van der Woude Syndrome

Author

Listed:
  • S. Karti

    (UHC Ibn Rochd, Morocco)

  • A. Chfiri

    (UHC Ibn Rochd, Morocco)

  • A. Jalal

    (UHC Ibn Rochd, Morocco)

  • A. El Harti

    (UHC Ibn Rochd, Morocco)

  • M. Diouri

    (UHC Ibn Rochd, Morocco)

Abstract

Van der Woude syndrome or lip pits syndrome is a rare genetic autosomal dominant affection that represents the first cause of syndromic cleft lip and palate. Lower lip pits associated or not with cleft lip or palate is characteristic in this syndrome. The treatment of lip pits is surgical and can be very challenging since aesthetic good results can be hard to achieve We report a familial case of Van der Woude syndrome with lip pits as the only manifestation.

Suggested Citation

  • S. Karti & A. Chfiri & A. Jalal & A. El Harti & M. Diouri, 2022. "Congenital Lower Lip Pits: A Familial Case of Van der Woude Syndrome," European Journal of Medical and Health Sciences, European Open Science, vol. 4(1), pages 38-40, January.
  • Handle: RePEc:epw:ejmed0:v:4:y:2022:i:1:id:41227
    DOI: 10.24018/ejmed.2022.4.1.1227
    as

    Download full text from publisher

    File URL: https://eu-opensci.org/index.php/ejmed/article/view/41227
    File Function: Abstract page
    Download Restriction: no

    File URL: https://eu-opensci.org/index.php/ejmed/article/download/41227/9402
    File Function: Full text
    Download Restriction: no

    File URL: https://libkey.io/10.24018/ejmed.2022.4.1.1227?utm_source=ideas
    LibKey link: if access is restricted and if your library uses this service, LibKey will redirect you to where you can use your library subscription to access this item
    ---><---

    More about this item

    Keywords

    ;
    ;
    ;
    ;

    Statistics

    Access and download statistics

    Corrections

    All material on this site has been provided by the respective publishers and authors. You can help correct errors and omissions. When requesting a correction, please mention this item's handle: RePEc:epw:ejmed0:v:4:y:2022:i:1:id:41227. See general information about how to correct material in RePEc.

    If you have authored this item and are not yet registered with RePEc, we encourage you to do it here. This allows to link your profile to this item. It also allows you to accept potential citations to this item that we are uncertain about.

    We have no bibliographic references for this item. You can help adding them by using this form .

    If you know of missing items citing this one, you can help us creating those links by adding the relevant references in the same way as above, for each refering item. If you are a registered author of this item, you may also want to check the "citations" tab in your RePEc Author Service profile, as there may be some citations waiting for confirmation.

    For technical questions regarding this item, or to correct its authors, title, abstract, bibliographic or download information, contact: Support (email available below). General contact details of provider: https://eu-opensci.org/index.php/ejmed .

    Please note that corrections may take a couple of weeks to filter through the various RePEc services.

    IDEAS is a RePEc service. RePEc uses bibliographic data supplied by the respective publishers.