Abstract
Ascher syndrome (Laffer-Ascher syndrome) is a rare disorder of unknown etiology, with a prevalence <1 case/million populations worldwide. The classical clinical triad is blepharochalasis, double lip and non-toxic thyroid enlargement. The syndrome can occur without nontoxic enlargement of the thyroid gland and is then considered as the forme fruste or incomplete form.
References
- Ascher KW. Blepharochalasismitstruma und doppellippe. Klin Monbl Augenheilkd 1920;65:85-9.
- Ramesh BA. Ascher syndrome: Review of literature and case report. Indian J PlastSurg2011;44:147-9
- Mühlendyck H, Hundeiker M. Blepharoachalasis (Fuchs) and the Laffer-Ascher syndrome. Hautarzt1978;29:474-7.
- Varshney AP, Gahalaut P, Mishra N, Rastogi MK. Ascher syndrome. Indian J Paediatr Dermatol. 2019;20:252-4.
- Chander R, Mal J, Jain A, Jaykar K. Ascher syndrome: A case report. Pediatr Dermatol2009;26:631-3.
- Zhai Z, Song, Hao F et al. Asher syndrome. Dermatologica Sinica 2015;33: 26-28.
Corresponding Author
Dr Shailja Chauhan
MD (Dermatology, Venereology and Leprosy), Civil Hospital, Rampur Bushar, District- Shimla, Himachal Pradesh