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Updated: Oct 8, 2026

In Vivo Functional Study of Disease-associated Rare Human Variants Using Drosophila
Published on: August 20, 2019
Two brothers with severe developmental delay, growth retardation and unusual appearance
E G Lemire1, G P Stoeber, M Anselmo
1Division of Medical Genetics, University of Saskatchewan & Royal University Hospital, Saskatoon, Canada. lemiree@sdh.sk.ca
Abstract:
We report on two brothers with short stature, severe developmental delay and unusual appearance. Several conditions including the Russell-Silver, Dubowitz, Floating-Harbour and Cockayne syndromes were considered in the differential diagnosis, but subsequently rejected. These two cases are likely to represent a new autosomal recessive or X-linked recessive syndrome.
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