|
|
The influence of genetic syndromes on the algorithm of cleft lip and palate repair : a retrospective study |
|---|---|
| Author: | Sándor-Bajusz, Kinga Amália1; Maros, Teodor Barna2; Olasz, Lajos3; |
| Organizations: |
1Departments of Paediatrics University of Pécs, Pécs, Hungary 2Department of Otorhinolaryngology, Ferenc Flór County Hospital, Kistarcsa 3Department of Dentistry, Oral and Maxillofacial Surgery, University of Pécs, Pécs, Hungary
4Department of Oral and Maxillofacial Surgery, Medical Research Centre, University of Oulu, Oulu University Hospital, Oulu, Finland
5Department of Medical Genetics, University of Pécs, Pécs, Hungary 6Paediatric Surgery, Department of Paediatrics, University of Pécs, Pécs, Hungary |
| Format: | article |
| Version: | published version |
| Access: | open |
| Online Access: | PDF Full Text (PDF, 1.1 MB) |
| Persistent link: | http://urn.fi/urn:nbn:fi-fe2021120859585 |
| Language: | English |
| Published: |
Wolters Kluwer,
2021
|
| Publish Date: | 2021-12-08 |
| Description: |
AbstractIntroduction: This study aimed to determine if the treatment algorithm used for nonsyndromic cleft patients required alteration to manage syndromic cleft lip and/or palate patients. Methods: The records of patients managed by the Pécs Cleft Team between January 1999 and December 2015 were analyzed retrospectively. The sources of the data included clinical and genetic records. Results: A total of 607 patients were managed by the cleft team during the study. Sixteen patients (2.6%) were noted to be afflicted with a particular identifiable syndrome. Seven different genetic syndromes and one sequence were present in the study. The Pierre Robin sequence occurred most often, comprising 50% of the cohort. The treatment algorithm used in managing nonsyndromic clefts required modification in 13 of the 16 syndromic patients. Discussion: The presence of a genetic syndrome may notably affect the treatment algorithm in children born with cleft lip and/or palate. The surgical treatment of certain associated anomalies has by necessity, priority over the timing of the reconstruction of the cleft lip and/or cleft palate in syndromic patients. see all
|
| Series: |
Annals of maxillofacial surgery |
| ISSN: | 2231-0746 |
| ISSN-E: | 2249-3816 |
| ISSN-L: | 2231-0746 |
| Volume: | In press |
| DOI: | 10.4103/ams.ams_77_21 |
| OADOI: | https://oadoi.org/10.4103/ams.ams_77_21 |
| Type of Publication: |
A1 Journal article – refereed |
| Field of Science: |
1184 Genetics, developmental biology, physiology |
| Subjects: | |
| Copyright information: |
© 2021 The Authors. This is an open access journal, and articles are distributed under the terms of the
Creative Commons Attribution‑NonCommercial‑ShareAlike 4.0 License, which
allows others to remix, tweak, and build upon the work non‑commercially, as long
as appropriate credit is given and the new creations are licensed under the identical
terms. |
|
https://creativecommons.org/licenses/by-nc-sa/4.0/ |