Olmsted syndrome: A case report and review of literature

Citations of this article
Mendeley users who have this article in their library.


© 2018 Indian Journal of Dermatology | Published by Wolters Kluwer - Medknow. H syndrome is a rare autosomal recessive syndrome characterised by constellation of clinical features and systemic manifestations including cutaneous hyperpigmentation, hypertrichosis, hepatosplenomegaly, hearing loss, heart anomalies, hypogonadism, hyperglycaemia, low height, and hallux valgus. We report a case of this syndrome with typical clinical findings. We report this case citing the rarity of this uncommon entity.




Tao, J., Huang, C. Z., Yu, N. W., Wu, Y., Liu, Y. Q., Li, Y., … Tu, Y. T. (2008, May). Olmsted syndrome: A case report and review of literature. International Journal of Dermatology. https://doi.org/10.1111/j.1365-4632.2008.03595.x

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free