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CASE REPORT
Year : 2020  |  Volume : 32  |  Issue : 4  |  Page : 405-407

Ascher Syndrome: A Case Report


1 Department of Oral Medicine and Radiology, Rural Dental College, Pravara Institute of Medical Sciences, Ahmednagar, Rahata, Loni, Maharashtra, India
2 Department of Oral Medicine and Radiology, SMBT Dental College, Dhamangaon, Nashik, Maharashtra, India

Correspondence Address:
Dr. Sunil S Mishra
Department of Oral Medicine and Radiology, Rural Dental College, Pravara Institute of Medical Sciences (Deemed University), Ahmednagar, Rahata, Loni - 413 736, Maharashtra
India
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/jiaomr.jiaomr_146_20

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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.


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