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Ophthalmic findings in Setleis syndrome: two new cases in a mother and son
Jerrod S Kent1, Kenneth G Romanchuk, Edmond G Lemire
1College of Medicine, University of Saskatchewan, Saskatoon, Sask.
Abstract
Case Report:
Setleis syndrome is a rare ectodermal dysplasia with characteristic ophthalmic findings. We describe the first 2 reported cases in Canadian individuals of Aboriginal descent.
Comments:
Although most ophthalmic findings are benign, it is important to recognize the clinical significance for management and genetic counselling. We postulate an autosomal dominant inheritance in our cases.
