Michels syndrome: the first case report from India and review of literature.

ABSTRACT: A 2-year 7-month-old girl born out of a consanguineous marriage, presented at our facility with clinical features characterized by the eyelid triad of blepharophimosis, blepharoptosis and epicanthus inversus in association with hypertelorism, cleft palate and craniosynostosis. This constellation of features is suggestive of Michels syndrome. At the time of writing this report, there were only ten reported cases worldwide and to the best of our knowledge, there have been no published reports from India.

SUBMITTER: Adio AA 

PROVIDER: S-EPMC4244746 | biostudies-literature | 2014 Sep

REPOSITORIES: biostudies-literature