Abstract
The Ascher or Laffe–Ascher syndrome is characterized by blepharochalasis, double lip and nontoxic thyroid enlargement. The syndrome is a rare manifestation and often remains undiagnosed. We report a case of Ascher syndrome in a 16 years old boy with double lip including upper and lower lip, blepharochalasis and an additional finding of mild clinodactyly which makes it a rare presentation. The article describes in brief an overview of the syndrome.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
More From: Journal of Indian Academy of Oral Medicine and Radiology
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.