A Family with Van der Woude Syndrome
The Van der Woude syndrome is a rare autosomal-dominant craniofacial disorder. In its classical form consisting of a cleft lip or cleft palate, distinctive pits of the lower lips and hypodontia. This is a review of a family with VWS. The family pedigree, past history and clinical features were revie...
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| Format: | Article |
| Language: | English |
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university of basrah
2006-06-01
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| Series: | Basrah Journal of Surgery |
| Subjects: | |
| Online Access: | https://bjsrg.uobasrah.edu.iq/article_55344_914a77c8d231729a563a9172c701d4e2.pdf |
| _version_ | 1811285662284906496 |
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| author | Zuhair F Fathallah |
| author_facet | Zuhair F Fathallah |
| author_sort | Zuhair F Fathallah |
| collection | DOAJ |
| description | The Van der Woude syndrome is a rare autosomal-dominant craniofacial disorder. In its classical form consisting of a cleft lip or cleft palate, distinctive pits of the lower lips and hypodontia. This is a review of a family with VWS. The family pedigree, past history and clinical features were reviewed. The related literatures were studied, which show the variable presentations including lip pits alone, absent teeth, or isolated cleft lip and palate of varying degrees of severity, and the points for early diagnosis. |
| first_indexed | 2024-04-13T02:48:24Z |
| format | Article |
| id | doaj.art-2bf143f2b51448d4a7cf586d383a2175 |
| institution | Directory Open Access Journal |
| issn | 1683-3589 2409-501X |
| language | English |
| last_indexed | 2024-04-13T02:48:24Z |
| publishDate | 2006-06-01 |
| publisher | university of basrah |
| record_format | Article |
| series | Basrah Journal of Surgery |
| spelling | doaj.art-2bf143f2b51448d4a7cf586d383a21752022-12-22T03:05:56Zenguniversity of basrahBasrah Journal of Surgery1683-35892409-501X2006-06-011210010.33762/bsurg.2006.5534455344A Family with Van der Woude SyndromeZuhair F FathallahThe Van der Woude syndrome is a rare autosomal-dominant craniofacial disorder. In its classical form consisting of a cleft lip or cleft palate, distinctive pits of the lower lips and hypodontia. This is a review of a family with VWS. The family pedigree, past history and clinical features were reviewed. The related literatures were studied, which show the variable presentations including lip pits alone, absent teeth, or isolated cleft lip and palate of varying degrees of severity, and the points for early diagnosis.https://bjsrg.uobasrah.edu.iq/article_55344_914a77c8d231729a563a9172c701d4e2.pdfvan der woude syndrome |
| spellingShingle | Zuhair F Fathallah A Family with Van der Woude Syndrome Basrah Journal of Surgery van der woude syndrome |
| title | A Family with Van der Woude Syndrome |
| title_full | A Family with Van der Woude Syndrome |
| title_fullStr | A Family with Van der Woude Syndrome |
| title_full_unstemmed | A Family with Van der Woude Syndrome |
| title_short | A Family with Van der Woude Syndrome |
| title_sort | family with van der woude syndrome |
| topic | van der woude syndrome |
| url | https://bjsrg.uobasrah.edu.iq/article_55344_914a77c8d231729a563a9172c701d4e2.pdf |
| work_keys_str_mv | AT zuhairffathallah afamilywithvanderwoudesyndrome AT zuhairffathallah familywithvanderwoudesyndrome |