“VAN DER WOUDE SYNDROME: REPORT OF TWO CASES”-Reference-Cited by-同舟云学术

“VAN DER WOUDE SYNDROME: REPORT OF TWO CASES”

Published:2021-06-01 Issue: Volume: Page:13-14
ISSN:
Container-title:INDIAN JOURNAL OF APPLIED RESEARCH
language:en
Short-container-title:IJAR

Author:

Sathish Sivan¹,Manonmani S.²,Mabel R. Christeffi³,Priyadharshini A.⁴

Affiliation:

1. MDS, MFDS, RCPS (Glasgow) (Professor and HOD); Department of Oral Medicine and Radiology.

2. (Post Graduate), Department of Oral Medicine and Radiology

3. MDS(Professor), Department of Oral Medicine and Radiology.

4. MDS (Senior lecturer), Department of Oral Medicine and Radiology.

Abstract

Van Der Woude syndrome is a rare autosomal dominant condition which is associated with developmental malformations involving lips, palate. This syndrome can be a genetic origin due to Microdeletion of chromosome bands 1q32-q41 and also mutation of Interferon regulatory factor 6 (IRF-6) can be a pathogenic cause. We report two interesting cases of Van Der Woude syndrome with lip pits and orofacial features.

Publisher

World Wide Journals

Reference8 articles.

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