'VAN DER WOUDE SYNDROME: REPORT OF TWO CASES'

Autor: Sivan Sathish, S. Manonmani, R. Christeffi Mabel, A. Priyadharshini
Rok vydání: 2021
Předmět:
Zdroj: INDIAN JOURNAL OF APPLIED RESEARCH. :13-14
Popis: 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.
Databáze: OpenAIRE